Rectal prolapse

Rectal prolapse
Classification and external resources
Specialty General surgery
ICD-10 K62.3
ICD-9-CM 569.1
OMIM 176780
DiseasesDB 11189
MedlinePlus 001132
eMedicine med/3533
Patient UK Rectal prolapse
MeSH D012005

Used colloquially, the term rectal prolapse often is used synonymously with complete rectal prolapse (external rectal prolapse), where the rectal walls have prolapsed to a degree where they protrude out the anus and are visible outside the body.[1] However, most researchers agree that there are 3 to 5 different types of rectal prolapse, depending on if the prolapsed section is visible externally, and if the full or only partial thickness of the rectal wall is involved.[2][3]

Rectal prolapse may occur without any symptoms, but depending upon the nature of the prolapse there may be mucous discharge (mucus coming from the anus), rectal bleeding, degrees of fecal incontinence and obstructed defecation symptoms.[4]

Rectal prolapse is generally more common in elderly women, although it may occur at any age and in both sexes. It is very rarely life-threatening, but the symptoms can be debilitating if left untreated.[4] Most external prolapse cases can be treated successfully, often with a surgical procedure. Internal prolapses are traditionally harder to treat and surgery may not be suitable for many patients.

Terminology

Prolapse refers to "the falling down or slipping of a body part from its usual position or relations". It is derived from the Latin pro- - "forward" + labi - "to slide". "Prolapse". Merriam-Webster Dictionary.  Prolapse can refer to many different medical conditions other than rectal prolapse.

procidentia has a similar meaning to prolapse, referring to "a sinking or prolapse of an organ or part". It is derived from the Latin procidere - "to fall forward".[5] Procidentia usually refers to uterine prolapse, but rectal procidentia can also be a synonym for rectal prolapse.

Intussusception is defined as invagination (infolding), especially referring to "the slipping of a length of intestine into an adjacent portion". It is derived from the Latin intus - "within" and susceptio - "action of undertaking", from suscipere - "to take up". "Intussusception". Merriam-Webster Dictionary.  Rectal intussusception is not to be confused with other intussusceptions involving colon or small intestine, which can sometimes be a medical emergency. Rectal intussusception by contrast is not life-threatening.

Intussusceptum refers to the proximal section of rectal wall, which telescopes into the lumen of the distal section of rectum (termed the intussuscipiens).[6] What results is 3 layers of rectal wall overlaid. From the lumen outwards, the first layer is the proximal wall of the intussusceptum, the middle is the wall of the intussusceptum folded back on itself, and the outer is the distal rectal wall, the intussuscipiens.[6]

Classification

A. Internal rectal intussusception. B. External (complete) rectal prolapse
A. full thickness external rectal prolapse, and B. mucosal prolapse. Note circumferential arrangement of folds in full thickness prolapse compared to radial folds in mucosal prolapse.[7]

The different kinds of rectal prolapse can be difficult to grasp, as different definitions are used and some recognize some subtypes and others do not. Essentially, rectal prolapses may be

External (complete) rectal prolapse (rectal procidentia, full thickness rectal prolapse, external rectal prolapse) is a full thickness, circumferential, true intussusception of the rectal wall which protrudes from the anus and is visible externally.[8][9]

Internal rectal intussusception (occult rectal prolapse, internal procidentia) can be defined as a funnel shaped infolding of the upper rectal (or lower sigmoid) wall that can occur during defecation.[10] This infolding is perhaps best visualised as folding a sock inside out,[6] creating "a tube within a tube".[11] Another definition is "where the rectum collapses but does not exit the anus".[12] Many sources differentiate between internal rectal intussusception and mucosal prolapse, implying that the former is a full thickness prolapse of rectal wall. However, a publication by the American society of colon and rectal surgeons stated that internal rectal intussusception involved the mucosal and submucosal layers separating from the underlying muscularis mucosa layer attachments, resulting in the separated portion of rectal lining “sliding” down.[4] This may signify that authors use the terms internal rectal prolapse and internal mucosal prolapse to describe the same phenomena.

Mucosal prolapse (partial rectal mucosal prolapse)[13] refers to prolapse of the loosening of the submucosal attachments to the muscularis propria of the distal rectummucosal layer of the rectal wall. Most sources define mucosal prolapse as an external, segmental prolapse which is easily confused with prolapsed (3rd or 4th degree) hemorrhoids (piles).[6] However, both internal mucosal prolapse (see below) and circumferential mucosal prolapse are described by some.[13] Others do not consider mucosal prolapse a true form of rectal prolapse.[14]

Internal mucosal prolapse (rectal internal mucosal prolapse, RIMP) refers to prolapse of the mucosal layer of the rectal wall which does not protrude externally. There is some controversy surrounding this condition as to its relationship with hemorrhoidal disease, or whether it is a separate entity.[15] The term "mucosal hemorrhoidal prolapse" is also used.[16]

Solitary rectal ulcer syndrome (SRUS, solitary rectal ulcer, SRU) occurs with internal rectal intussusception and is part of the spectrum of rectal prolapse conditions.[4] It describes ulceration of the rectal lining caused by repeated frictional damage as the internal intussusception is forced into the anal canal during straining. SRUS can be considered a consequence of internal intussusception, which can be demonstrated in 94% of cases.

Mucosal prolapse syndrome (MPS) is recognized by some. It includes solitary rectal ulcer syndrome, rectal prolapse, proctitis cystica profunda, and inflammatory polyps.[17][18] It is classified as a chronic benign inflammatory disorder.

Rectal prolapse and internal rectal intussusception has been classified according to the size of the prolapsed section of rectum, a function of rectal mobility from the sacrum and infolding of the rectum. This classification also takes into account sphincter relaxation:[19]

Rectal internal mucosal prolapse has been graded according to the level of descent of the intussusceptum, which was predictive of symptom severity:[20]

The most widely used classification of internal rectal prolapse is according to the height on the rectal/sigmoid wall from which they originate and by whether the intussusceptum remains within the rectum or extends into the anal canal. The height of intussusception from the anal canal is usually estimated by defecography.[11]

Recto-rectal (high) intussusception (intra-rectal intussusception) is where the intussusception starts in the rectum, does not protrude into the anal canal, but stays within the rectum. (i.e. the intussusceptum originates in the rectum and does not extend into the anal canal. The intussuscipiens includes rectal lumen distal to the intussusceptum only). These are usually intussusceptions that originate in the upper rectum or lower sigmoid.[11]

Recto-anal (low) intussusception (intra-anal intussusception) is where the intussusception starts in the rectum and protrudes into the anal canal (i.e. the intussusceptum originates in the rectum, and the intussuscipiens includes part of the anal canal)

An Anatomico-Functional Classification of internal rectal intussusception has been described,[11] with the argument that other factors apart from the height of intussusception above the anal canal appear to be important to predict symptomology. The parameters of this classification are anatomic descent, diameter of intussuscepted bowel, associated rectal hyposensitivity and associated delayed colonic transit:

Diagnosis

History

Patients may have associated gynecological conditions which may require multidisciplinary management.[4] History of constipation is important because some of the operations may worsen constipation. Fecal incontinence may also influence the choice of management.

Physical examination

Rectal prolapse may be confused easily with prolapsing hemorrhoids.[4] Mucosal prolapse also differs from prolapsing (3rd or 4th degree) hemorrhoids, where there is a segmental prolapse of the hemorrhoidal tissues at the 3,7 and 11’O clock positions.[13] Mucosal prolapse can be differentiated from a full thickness external rectal prolapse (a complete rectal prolapse) by the orientation of the folds (furrows) in the prolapsed section. In full thickness rectal prolapse, these folds run circumferential. In mucosal prolapse, these folds are radially.[6] The folds in mucosal prolapse are usually associated with internal hemorrhoids. Furthermore, in rectal prolapse, there is a sulcus present between the prolapsed bowel and the anal verge, whereas in hemorrhoidal disease there is no sulcus.[2] Prolapsed, incarcerated hemorrhoids are extremely painful, whereas as long as a rectal prolapse is not strangulated, it gives little pain and is easy to reduce.[4]

The prolapse may be obvious, or it may require straining and squatting to produce it.[4] The anus is usually patulous, (loose, open) and has reduced resting and squeeze pressures.[4] Sometimes it is necessary to observe the patient while they strain on a toilet to see the prolapse happen[21] (the perineum can be seen with a mirror or by placing an endoscope in the bowl of the toilet).[6] A phosphate enema may need to be used to induce straining.[2]

The perianal skin may be macerated (softening and whitening of skin that is kept constantly wet) and show excoriation.[6]

Proctoscopy/sigmoidoscopy/colonoscopy

These may reveal congestion and edema (swelling) of the distal rectal mucosa,[21] and in 10-15% of cases there may be a solitary rectal ulcer on the anterior rectal wall.[4] Localized inflammation or ulceration can be biopsied, and may lead to a diagnosis of SRUS or colitis cystica profunda.[4] Rarely, a neoplasm (tumour) may form on the leading edge of the intussusceptum. In addition, patients are frequently elderly and therefore have increased incidence of colorectal cancer. Full length colonoscopy is usually carried out in adults prior to any surgical intervention.[4] These investigations may be used with contrast media (barium enema) which may show the associated mucosal abnormalities.[6]

Videodefecography

This investigation is used to diagnose internal intussusception, or demonstrate a suspected external prolapse that could not be produced during the examination.[2] It is usually not necessary with obvious external rectal prolapse.[6] Defecography may demonstrate associated conditions like cystocele, vaginal vault prolapse or enterocele.[4]

Colonic transit studies

Colonic transit studies may be used to rule out colonic inertia if there is a history of severe constipation.[2][4] Continent prolapse patients with slow transit constipation, and who are fit for surgery may benefit from subtotal colectomy with rectopexy.[4]

Anorectal manometry

This investigation objectively documents the functional status of the sphincters. However, the clinical significance of the findings are disputed by some.[6] It may be used to assess for pelvic floor dyssenergia,[4] (anismus is a contraindication for certain surgeries, e.g. STARR), and these patients may benefit from post-operative biofeedback therapy. Decreased squeeze and resting pressures are usually the findings, and this may predate the development of the prolapse.[4] Resting tone is usually preserved in patients with mucosal prolapse.[21] In patients with reduced resting pressure, levatorplasty may be combined with prolapse repair to further improve continence.[6]

Anal electromyography/Pudendal nerve testing

May be used to evaluate incontinence, but there is disagreement about what relevance the results may show, as rarely do they mandate a change of surgical plan.[4] There may be denervation of striated musculature on the electromyogram.[21] Increased nerve conduction periods (nerve damage), this may be significant in predicting post-operative incontinence.[4]

Complete rectal prolapse

A severe example of complete (external) rectal prolapse. Note circumferential arrangement of mucosal folds.

Rectal prolapse is a “ falling down” of the rectum so that it is visible externally. The appearance is of a reddened, proboscis-like object through the anal sphincters. Patients find the condition embarrassing.[6] The symptoms can be socially debilitating without treatment,[4] but it is rarely life-threatening.[6]

The true incidence of rectal prolapse is unknown, but it is thought to be uncommon. As most sufferers are elderly, the condition is generally under-reported.[22] It may occur at any age, even in children,[23] but there is peak onset in the fourth and seventh decades.[2] Women over 50 are six times more likely to develop rectal prolapse than men. It is rare in men over 45 and in women under 20.[21] When males are affected, they tend to be young and report significant bowel function symptoms, especially obstructed defecation,[4] or have a predisposing disorder (e.g., congenital anal atresia).[6] When children are affected, they are usually under the age of 3.

35% of women with rectal prolapse have never had children,[4] suggesting that pregnancy and labour are not significant etiological factors. Anatomical differences such as the wider pelvic outlet in females may explain the skewed gender distribution.[6]

Associated conditions, especially in younger patients include autism, developmental delay syndromes and psychiatric conditions requiring several medications.[4]

Signs and symptoms

Signs and symptoms include:

Initially, the mass may protrude through the anal canal only during defecation and straining, and spontaneously return afterwards. Later, the mass may have to be pushed back in following defecation. This may progress to a chronically prolapsed and severe condition, defined as spontaneous prolapse that is difficult to keep inside, and occurs with walking, prolonged standing,[4] coughing or sneezing (Valsalva maneuvers).[2] A chronically prolapsed rectal tissue may undergo pathological changes such as thickening, ulceration and bleeding.[4]

If the prolapse becomes trapped externally outside the anal sphincters, it may become strangulated and there is a risk of perforation.[21] This may require an urgent surgical operation if the prolapse cannot be manually reduced.[4] Applying granulated sugar on the exposed rectal tissue can reduce the edema (swelling) and facilitate this.[21]

Cause

Micrograph showing a rectal wall with changes seen in rectal prolapse. There is a marked increase of fibrous tissue in the submucosa and fibrous tissue +/- smooth muscle hyperplasia in the lamina propria. H&E stain

The precise cause is unknown,[2][6][10] and has been much debated.[4] In 1912 Moschcowitzl proposed that rectal prolapse was a sliding hernia through a pelvic fascial defect.[6]

This theory was based on the observation that rectal prolapse patients have a mobile and unsupported pelvic floor, and a hernia sac of peritoneum from the Pouch of Douglas and rectal wall can be seen.[4] Other adjacent structures can sometimes be seen in addition to the rectal prolapse.[4] Although a pouch of Douglas hernia, originating in the cul de sac of Douglas, may protrude from the anus (via the anterior rectal wall),[21] this is a different situation from rectal prolapse.

Shortly after the invention of defecography, In 1968 Broden and Snellman used cinedefecography to show that rectal prolapse begins as a circumferential intussusception of the rectum,[2][6] which slowly increases over time.[21] The leading edge of the intussusceptum may be located at 6–8 cm or at 15–18 cm from the anal verge.[21] This proved an older theory from the 18th century by John Hunter and Albrecht von Haller that this condition is essentially a full-thickness rectal intussusception, beginning about 3 inches above the dentate line and protruding externally.[4]

Since most patients with rectal prolapse have a long history of constipation,[6] it is thought that prolonged, excessive and repetitive straining during defecation may predispose to rectal prolapse.[2][10][21][24][25][26] Since rectal prolapse itself causes functional obstruction, more straining may result from a small prolapse, with increasing damage to the anatomy.[10] This excessive straining may be due to predisposing pelvic floor dysfunction (e.g. obstructed defecation) and anatomical factors:[6][21]

Some authors question whether these abnormalities are the cause, or secondary to the prolapse.[2] Other predisposing factors/associated conditions include:

The association with uterine prolapse (10-25%) and cystocele (35%) may suggest that there is some underlying abnormality of the pelvic floor that affects multiple pelvic organs.[2] Proximal bilateral pudendal neuropathy has been demonstrated in patients with rectal prolapse who have fecal incontinence.[4] This finding was shown to be absent in healthy subjects, and may be the cause of denervation-related atrophy of the external anal sphincter. Some authors suggest that pudendal nerve damage is the cause for pelvic floor and anal sphincter weakening, and may be the underlying cause of a spectrum of pelvic floor disorders.[4]

Sphincter function in rectal prolapse is almost always reduced.[2] This may be the result of direct sphincter injury by chronic stretching of the prolapsing rectum. Alternatively, the intussuscepting rectum may lead to chronic stimulation of the rectoanal inhibitory reflex (RAIR - contraction of the external anal sphincter in response to stool in the rectum). The RAIR was shown to be absent or blunted. Squeeze (maximum voluntary contraction) pressures may be effected as well as the resting tone. This is most likely a denervation injury to the external anal sphincter.[2]

The assumed mechanism of fecal incontinence in rectal prolapse is by the chronic stretch and trauma to the anal sphincters and the presence of a direct conduit (the intussusceptum) connecting rectum to the external environment which is not guarded by the sphincters.[4]

The assumed mechanism of obstructed defecation is by disruption to the rectum and anal canal's ability to contract and fully evacuate rectal contents. The intussusceptum itself may mechanically obstruct the rectoanal lumen, creating a blockage that straining, anismus and colonic dysmotility exacerbate.[4]

Some believe that internal rectal intussusception represents the initial form of a progressive spectrum of disorders the extreme of which is external rectal prolapse. The intermediary stages would be gradually increasing sizes of intussusception. However, internal intussusception rarely progresses to external rectal prolapse.[28] The factors that result in a patient progressing from internal intussusception to a full thickness rectal prolapse remain unknown.[4] Defecography studies demonstrated that degrees of internal intussusception are present in 40% of asymptomatic subjects, raising the possibility that it represents a normal variant in some, and may predispose patients to develop symptoms, or exacerbate other problems.[29]

Treatment

Conservative

The only potentially curative treatment for complete rectal prolapse is surgery,[8] however in those patients with medical problems that make them unfit for surgery, and those patients who have minimal symptoms, conservative measures may benefit. Dietary adjustments, including increasing dietary fiber may be beneficial to reduce constipation,[8] and thereby reduce straining. A bulk forming agent (e.g. psyllium) or stool softener can also reduce constipation. Biofeedback retraining may be indicated to help the patient avoid straining during defecation. There is limited evidence that hypopressive exercises may be beneficial in mild pelvic organ prolapse.

Surgical

Surgery is often required to prevent further damage to the anal sphincters. The goals of surgery are to restore the normal anatomy and to minimize symptoms. There is no globally agreed consensus as to which procedures are more effective,[8] and there have been over 50 different operations described.[4]

Surgical approaches in rectal prolapse can be either perineal or abdominal. A perineal approach (or trans-perineal) refers to surgical access to the rectum and sigmoid colon via incision around the anus and perineum (the area between the genitals and the anus).[30] Abdominal approach (trans-abdominal approach) involves the surgeon cutting into the abdomen and gaining surgical access to the pelvic cavity. Procedures for rectal prolapse may involve fixation of the bowel (rectopexy), or resection (a portion removed), or both.[8] Trans-anal (endo-anal) procedures are also described where access to the internal rectum is gained through the anus itself.

Abdominal procedures

The abdominal approach carries a small risk of impotence in males (e.g. 1-2% in abdominal rectopexy).[6] Abdominal operations may be open or laparoscopic (keyhole surgery).[2]

Laproscopic procedures Recovery time following laparoscopic surgery is shorter and less painful than following traditional abdominal surgery.[30] Instead of opening the pelvic cavity with a wide incision (laparotomy), a laparoscope (a thin, lighted tube) and surgical instruments are inserted into the pelvic cavity via small incisions.[30] Rectopexy and anterior resection have been performed laparoscopically with good results.

Perineal procedures

The perineal approach generally results in less post-operative pain and complications, and a reduced length of hospital stay. These procedures generally carry a higher recurrence rate and poorer functional outcome.[4] The perineal procedures include perineal rectosigmoidectomy and Delorme repair.[2] Elderly, or other medically high-risk patients are usually treated by perineal procedures,[2] as they can be performed under a regional anesthetic, or even local anesthetic with intravenous sedation, thus avoid the risks of a general anesthetic.[6] Alternatively, perineal procedures may be selected to reduce risk of nerve damage, for example in young male patients for whom sexual dysfunction may be a major concern.[4]

Perineal rectosigmoidectomy

Perineal rectosigmoidectomy aims to resect (remove) the redundant bowel via the perineum and anchor the lower rectum to the sacrum through fibrosis in the hope of preventing future prolapse.[8] The full thickness of the rectal wall is incised at a level just above the dentate line. Redundant rectal and sigmoid wall is removed and the new edge of colon is reconnected (anastomosed) with the anal canal with stitches or staples.[6] This procedure may be combined with a procedure to tighten the pelvic muscles (levatorplasty).[8] A combined a perineal proctosigmoidectomy with anterior levatoroplasty is also called an Altemeier procedure.[2] Levatorplasty is performed to correct elvator diastasis which is commonly associated with rectal prolapse.[2] Perineal rectosigmoidectomy was first introduced by Mikulicz in 1899, and it remained the preferred treatment in Europe for many years.[2] It was Popularized by Altemeier.[6] The procedure is simple, safe and effective.[2] Continence Levatorplasty may enhance restoration of continence (2/3 of patients).[2] Complications occur in less than 10% of cases, and include pelvic bleeding, pelvic abscess and anastomotic dehiscence (splitting apart of the stitches inside), bleeding or leak at a dehiscence[2] Mortality is low.[6] Recurrence rates are higher than for abdominal repair,[2] 16-30%, but more recent studies give lower recurrence rates.[2] Additional levatoroplasty can reduce recurrence rates to 7%.[2]

Delorme Procedure

This is a modification of the perineal rectosigmoidectomy, differing in that only the mucosa and submucosa are excised from the prolapsed segment, rather than full thickness resection.[6] The prolapse is exposed if it is not already present, and the mucosal and submucosal layers are stripped from the redundant length of bowel. The muscle layer that is left is plicated (folded) and placed as a buttress above the pelvic floor.[8] The edges of the mucosal are then stitched back together. "Mucosal proctectomy" was first discussed by Delorme in 1900,[6] now it is becoming more popular again as it has low morbidity and avoids an abdominal incision, while effectively repairing the prolapse.[2] The procedure is ideally suited to those patients with full-thickness prolapse limited to partial circumference (e.g., anterior wall) or less-extensive prolapse (perineal rectosigmoidectomy may be difficult in this situation).[2][6] Fecal incontinence is improved following surgery (40%–75% of patients).[4][6] Post operatively, both mean resting and squeeze pressures were increased.[4] Constipation is improved in 50% of cases,[4] but often urgency and tenesmus are created. Complications, including infection, urinary retention, bleeding, anastomotic dehiscence (opening of the stitched edges inside), stricture (narrowing of the gut lumen), diarrhea, and fecal impaction occur in 6-32% of cases.[4][6] Mortality occurs in 0-2.5% cases.[6] There is a higher recurrence rate than abdominal approaches (7-26% cases).[4][6]

Anal encirclement (Thirsch procedure)

This procedure can be carried out under local anaesthetic. After reduction of the prolapse, a subcutaneous suture (a stich under the skin) or other material is placed encircling the anus, which is then made taut to prevent further prolapse.[8] Placing silver wire around the anus first described by Thiersch in 1891.[6] Materials used include nylon, silk, silastic rods, silicone, Marlex mesh, Mersilene mesh, fascia, tendon, and Dacron.[6] This operation does not correct the prolapse itself, it merely supplements the anal sphincter, narrowing the anal canal with the aim of preventing the prolapse from becoming external, meaning it remains in the rectum.[6] This goal is achieved in 54-100% cases. Complications include breakage of the encirclement material, fecal impaction, sepsis, and erosion into the skin or anal canal. Recurrence rates are higher that the other perineal procedures. This procedure is generally reserved for debilitated or other individuals at high anesthetic risk,[8] who may not tolerate other perineal procedures.

Internal rectal intussusception

Internal rectal intussusception (rectal intussusception, internal intussusception, internal rectal prolapse, occult rectal prolapse, internal rectal procidentia and rectal invagination) is a medical condition defined as a funnel shaped infolding of the rectal wall that can occur during defecation.[10]

This phenomenon was first described in the late 1960s when defecagraphy was first developed and became widespread.[4] Degrees of internal intussusception have been demonstrated in 40% of asymptomatic subjects, raising the possibility that it represents a normal variant in some, and may predispose patients to develop symptoms, or exacerbate other problems.[29]

Symptoms

Internal intussusception may be asymptomatic, but common symptoms include:[2]

Recto-rectal intussusceptions may be asymptomatic, apart from mild obstructed defecation. "interrupted defaecation" in the morning is thought by some to be characteristic.[11]

Recto-anal intussusceptions commonly give more severe symptoms of straining, incomplete evacuation, need for digital evacuation of stool, need for support of the perineum during defecation, urgency, frequency or intermittent fecal incontinence.[11]

It has been observed that intussusceptions of thickness ≥3 mm, and those that appear to cause obstruction to rectal evacuation may give clinical symptoms.[33][34]

Etiology

There are 2 schools of thought regarding the nature of internal intussusception, viz: whether it is a primary phenomenon, or secondary to (a consequence of) another condition.

Some believe that it represents the initial form of a progressive spectrum of disorders the extreme of which is external rectal prolapse. The intermediary stages would be gradually increasing sizes of intussusception. The folding section of rectum can cause repeated trauma to the mucosa, and can cause solitary rectal ulcer syndrome.[6] However, internal intussusception rarely progresses to external rectal prolapse.[28]

Others argue that the majority of patients appear to have rectal intussusception as a consequence of obstructed defecation rather than a cause,[35][36] possibly related to excessive straining in patients with obstructed defecation.[33] Patients with other causes of obstructed defecation (outlet obstruction) like anismus also tend to have higher incidence of internal intussusception. Enteroceles are coexistent in 11% of patients with internal intussusception.[37] Symptoms of internal intussusception overlap with those of rectocele, indeed the 2 conditions can occur together.[38]

Patients with solitary rectal ulcer syndrome combined with internal intussusception (as 94% of SRUS patients have) were shown to have altered rectal wall biomechanics compared to patients with internal intussusception alone.[39] The presumed mechanism of the obstructed defecation is by telescoping of the intussusceptum, occluding the rectal lumen during attempted defecation.[33] One study analysed resected rectal wall specimens in patients with obstructed defecation associated with rectal intussusception undergoing stapled trans-anal rectal resection. They reported abnormalities of the enteric nervous system and estrogen receptors.[40] One study concluded that intussusception of the anterior rectal wall shares the same cause as rectocele, namely deficient recto-vaginal ligamentous support.[41]

Comorbidities & complications

The following conditions occur more commonly in patients with internal rectal intussusception than in the general population:

Diagnosis

Unlike external rectal prolapse, internal rectal intussusception is not visible externally, but it may still be diagnosed by digital rectal examination, while the patient strains as if to defecate.[11] Imaging such as a defecating proctogram[44] or dynamic MRI defecography can demonstrate the abnormal folding of the rectal wall. Some have advocated the use of anorectal physiology testing (anorectal manometry).[4]

Treatment

Non surgical measures to treat internal intussusception include pelvic floor retraining,[45] a bulking agent (e.g. psyllium), suppositories or enemas to relieve constipation and straining.[21] If there is incontinence (fecal leakage or more severe FI), or paradoxical contraction of the pelvic floor (anismus), then biofeedback retraining is indicated.[46] Some researchers advise that internal intussusception be managed conservatively, compared to external rectal prolapse which usually requires surgery.[47]

As with external rectal prolapse, there are a great many different surgical interventions described. Generally, a section of rectal wall can be resected (removed), or the rectum can be fixed (rectopexy) to its original position against the sacral vertebrae, or a combination of both methods. Surgery for internal rectal prolapse can be via the abdominal approach or the transanal approach.[48]

It is clear that there is a wide spectrum of symptom severity, meaning that some patients may benefit from surgery and others may not. Many procedures receive conflicting reports of success, leading to a lack of any consensus about the best way to manage this problem.[46] Relapse of the intussusception after treatment is a problem. Two of the most commonly employed procedures are discussed below.

laparoscopic ventral (mesh) rectopexy (LVR)

This procedure aims to "[correct] the descent of the posterior and middle pelvic compartments combined with reinforcement of the rectovaginal septum".[48]

Rectopexy has been shown to improve anal incontinence (fecal leakage) in patients with rectal intussusception.[49] The operation has been shown to have low recurrence rate (around 5%).[50] It also improves obstructed defecation symptoms.[51]

Complications include constipation, which is reduced if the technique does not use posterior rectal mobilization (freeing the rectum from its attached back surface).[52]

The advantage of the laproscopic approach is decreased healing time and less complications.[50]

Stapled trans-anal rectal resection (STARR)

This operation aims to "remove the anorectal mucosa circumferential and reinforce the anterior anorectal junction wall with the use of a circular stapler".[42][43] In contrast to other methods, STARR does not correct the descent of the rectum, it removes the redundant tissue.[48] The technique was developed from a similar stapling procedure for prolapsing hemorrhoids. Since, specialized circular staplers have been developed for use in external rectal prolapse and internal rectal intussusception.[53]

Complications, sometimes serious, have been reported following STARR,[54][55][55][56][57][58] but the procedure is now considered safe and effective.[57] STARR is contraindicated in patients with weak sphincters (fecal incontinence and urgency are a possible complication) and with anismus (paradoxical contraction of the pelvic floor during attempted defecation).[57] The operation has been shown to improve rectal sensitivity and decrease rectal volume, the reason thought to create urgency.[48] 90% of patients do not report urgency 12 months after the operation. The anal sphincter may also be stretched during the operation. STARR was compared with biofeedback and found to be more effective at reducing symptoms and improving quality of life.[59]

Mucosal prolapse

Rectal mucosal prolapse (mucosal prolapse, anal mucosal prolapse) is a sub-type of rectal prolapse, and refers to abnormal descent of the rectal mucosa through the anus.[21] It is different to an internal intussusception (occult prolapse) or a complete rectal prolapse (external prolapse, procidentia) because these conditions involve the full thickness of the rectal wall, rather than only the mucosa (lining).[13]

Mucosal prolapse is a different condition to prolapsing (3rd or 4th degree) hemorrhoids,[13] although they may look similar.

Rectal mucosal prolapse can be a cause of obstructed defecation (outlet obstruction).[10] and rectal malodor.

Symptoms

Symptom severity increases with the size of the prolapse, and whether it spontaneously reduces after defecation, requires manual reduction by the patient, or becomes irreducible. The symptoms are identical to advanced hemorrhoidal disease,[13] and include:

Etiology

The condition, along with complete rectal prolapse and internal rectal intussusception, is thought to be related to chronic straining during defecation and constipation.

Mucosal prolapse occurs when the results from loosening of the submucosal attachments (between the mucosal layer and the muscularis propria) of the distal rectum.[2] The section of prolapsed rectal mucosa can become ulcerated, leading to bleeding.

Diagnosis

Mucosal prolapse can be differentiated from a full thickness external rectal prolapse (a complete rectal prolapse) by the orientation of the folds (furrows) in the prolapsed section. In full thickness rectal prolapse, these folds run circumferential. In mucosal prolapse, these folds are radially.[6] The folds in mucosal prolapse are usually associated with internal hemorrhoids.[21]

Treatment

EUA (examination under anesthesia) of anorectum and banding of the mucosa with rubber bands

Solitary rectal ulcer syndrome & colitis cystica profunda

Solitary rectal ulcer syndrome (SRUS, SRU), is a disorder of the rectum and anal canal, caused by straining and increased pressure during defecation. This increased pressure causes the anterior portion of the rectal lining to be forced into the anal canal (an internal rectal intussusception). The lining of the rectum is repeatedly damaged by this friction, resulting in ulceration. SRUS can therefore considered to be a consequence of internal intussusception (a sub type of rectal prolapse), which can be demonstrated in 94% of cases. It may be asymptomatic, but it can cause rectal pain, rectal bleeding, rectal malodor, incomplete evacuation and obstructed defecation (rectal outlet obstruction).

Symptoms

Symptoms include:[18][21][60]

Prevalence

The condition is thought to be uncommon. It usually occurs in young adults, but children can be affected too.[61]

Etiology

The essential cause of SRUS is thought to be related to too much straining during defecation.

Overactivity of the anal sphincter during defecation causes the patient to require more effort to expel stool. This pressure is produced by the modified valsalva manovoure (attempted forced exhalation against a closed glottis, resulting in increased abdominal and intra-rectal pressure). Patiest with SRUS were shown to have higher intra-rectal pressures when straining than healthy controls.[62] SRUS is also associated with prolonged and incomplete evacuation of stool.[63]

More effort is required because of concomitant anismus, or non-relaxation/paradoxical contraction of puborectalis (which should normally relax during defecation).[64] The increased pressure forces the anterior rectal lining against the contracted puborectalis and frequently the lining prolapses into the anal canal during straining and then returns to its normal position afterwards.

The repeated trapping of the lining can cause the tissue to become swollen and congested. Ulceration is thought to be caused by resulting poor blood supply (ischemia), combined with repeated frictional trauma from the prolapsing lining, and exposure to increased pressure are thought to cause ulceration. Trauma from hard stools may also contribute.

The site of the ulcer is typically on the anterior wall of the rectal ampulla, about 7–10 cm from the anus. However, the area may of ulceration may be closer to the anus, deeper inside, or on the lateral or posterior rectal walls. The name "solitary" can be misleading since there may be more than one ulcer present. Furthermore, there is a "preulcerative phase" where there is no ulcer at all.[65]

Pathological specimens of sections of rectal wall taken from SRUS patients show thickening and replacement of muscle with fibrous tissue and excess collagen.[66] Rarely, SRUS can present as polyps in the rectum.[67][68]

SRUS is therefore associated and with internal, and more rarely, external rectal prolapse.[63] Some believe that SRUS represents a spectrum of different diseases with different etiologies.[69]

Another condition associated with internal intussusception is colitis cystica profunda (also known as CCP, or proctitis cystica profunda), which is cystica profunda in the rectum. Cystica profunda is characterized by formation of mucin cysts in the muscle layers of the gut lining, and it can occur anywhere along the gastrointestinal tract. When it occurs in the rectum, some believe to be an interchangeable diagnosis with SRUS since the histologic features of the conditions overlap.[70][71] Indeed, CCP is managed identically to SRUS.[72]

Electromyography may show pudendal nerve motor latency.[18]

Complications

Complications are uncommon, but include massive rectal bleeding, ulceration into the prostate gland or formation of a stricture.[73][74][75] Very rarely, cancer can arise on the section of prolapsed rectal lining.[17]

Diagnosis and investigations

SRUS is commonly misdiagnosed, and the diagnosis is not made for 5–7 years.[61] Clinicians may not be familiar with the condition, and treat for Inflammatory bowel disease, or simple constipation.[76][77]

The thickened lining or ulceration can also be mistaken for types of cancer.[78][79][80][81]

The differential diagnosis of SRUS (and CCP) includes:[6]

Defecography, sigmoidoscopy, transrectal ultrasound, mucosal biopsy, anorectal manometry and electromyography have all been used to diagnose and study SRUS.[18][64] Some recommend biopsy as essential for diagnosis since ulcerations may not always be present, and others state defecography as the investigation of choice to diagnose SRUS.[60][71][76]

Treatment

Although SRUS is not a medically serious disease, it can be the cause of significantly reduced quality of life for patients. It is difficult to treat, and treatment is aimed at minimizing symptoms.

Stopping straining during bowel movements, by use of correct posture, dietary fiber intake (possibly included bulk forming laxatives such as psyllium), stool softeners (e.g. polyethylene glycol,[82][83] and biofeedback retraining to coordinate pelvic floor during defecation.[84][85]

Surgery may be considered, but only if non surgical treatment has failed and the symptoms are severe enough to warrant the intervention. Improvement with surgery is about 55-60%.[86]

Ulceration may persist even when symptoms resolve.[87]

Mucosal prolapse syndrome

A group of conditions known as Mucosal prolapse syndrome (MPS) has now been recognized. It includes SRUS, rectal prolapse, proctitis cystica profunda, and inflammatory polyps.[17][18] It is classified as a chronic benign inflammatory disorder. The unifying feature is varying degrees of rectal prolapse, whether internal intussusception (occult prolapse) or external prolapse.

Pornography

"Rosebudding" is so called as the appearance of the exposed rectum is said to resemble rosebud flowers.

Rosebud pornography, rosebudding or rectal prolapse pornography refers to an anal sex practice which occurs in some extreme anal pornography whereby a pornograhic actor or actress performs a rectal prolapse whereby the walls of the rectum slip out of the anus. A rectal prolapse is a serious medical condition that requires the attention of a medical professional. However, in rosebud pornography it is performed deliberately. Michelle Lhooq, writing for VICE, argues that rosebudding is an example of producers making 'extreme' content due to the easy availability of free pornography on the internet. She also argues that rosebudding is a way for pornographic actors and actresses to distinguish themselves.[88] Repeated rectal prolapses can cause bowel problems and anal leakage and therefore risk the health of pornographic actors or actresses who participate in them.[89] Lhooq also argues that some who participate in this form of pornography are unaware of the consequences.[89]

See also

External links

References

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