A 34-year-old Hispanic man presented to the emergency department
with a 3-week history of postprandial nausea and bilious emesis. He
had no significant medical history except for a superficial gunshot
wound to the left flank several years previously, in which the
bullet did not perforate the peritoneum. He had no history of prior
abdominal surgery. Physical examination was positive for a
nondiscrete palpable mass at the midepigastrium and right upper
quadrant, which was moderately tender to palpation. Bowel sounds
were mildly hyperactive. Laboratory findings revealed a profound
metabolic alkalosis with hypokalemia. Esophagogastroduodenoscopy
(EGD) showed distended fluid-filled stomach and duodenum.
Radiological workup included computed tomography (CT) scanning of
the abdomen and pelvis. The patient did not improve on conservative
management, and on day 7 of his hospitalization, he was taken to
the operating room for exploratory laparotomy.
Diagnosis
Abdominal Cocoon
Findings
A contrast-enhanced CT scan of the abdomen and pelvis showed a
markedly distended stomach and proximal small bowel, with the small
bowel loops clustered together and displaced into the right upper
quadrant and right mid-abdomen (Figure 1). The overlying peritoneum
was thickened and pockets of fluid were present in the jejunal
mesentery. Intraoperative ultrasound showed clumped small bowel
with thickened surrounding peritoneum (Figure 2). Interoperative
Findings Exploratory laparotomy revealed a large mass of small
bowel surrounded by a thick inflammatory rind with multiple
adhesions, encompassing approximately 90% of the bowel. Pathology
Lysed pseudocapsule showed dense fibrosis with chronic inflammation
and hemorrhage.
Discussion
Abdominal cocoon syndrome is a rare entity that is also known in
the literature as sclerosing peritonitis or sclerosing
encapsulating peritonitis.1 It is characterized by partial or
complete encasement of small bowel by a thick rind of fibrous
tissue and adhesions, causing clustering of the bowel.
Occasionally, the large bowel, stomach, or other abdominal organs
may be involved.2 Clinically, the condition may present with vague
abdominal pain and weight loss. For patients who are on chronic
ambulatory peritoneal dialysis (CAPD), there is a loss of
ultrafiltration capacity and a bloody dialysis effluent. However,
early clinical features of sclerosing peritonitis are generally
nonspecific and are frequently not recognized until the patient
develops partial or complete small bowel obstruction.3 The
characteristic radiologic findings of sclerosing peritonitis have
been sparsely described. Ultrasound may show clumping of bowel
loops with the bowel surrounded by a thick rim of hypoechoic
tissue. Tethering of the bowel posteriorly, or the presence of a
membrane anterior to the small bowel may be seen.1,4 Barium studies
show varying length of small bowel tightly enclosed in a thickened
peritoneum, proximal small bowel dilation, and an increase in
transit time.5 The CT findings may also include an encapsulated
clump of bowel, peritoneal thickening, calcification, peritoneal
enhancement, small bowel tethering, and loculated fluid
collections.1,3 Peritoneal calcification and tethering of the small
bowel loops are associated more specifically with sclerosing
peritonitis than the other CT findings.6 Multiple etiologies for
abdominal cocoon have been established, although the underlying
pathogenesis is not fully understood. It may occur as a serious
complication of CAPD.5 It has also been described in association
with prolonged practolol therapy, sarcoidosis, systemic lupus
erythematosus, indwelling abdominal catheters (specifically Le-Veen
shunts), orthotopic liver transplantation, and tuberculous pelvic
inflammatory disease.1,7-10 These conditions may predispose
patients to peritoneal irritation and inflammation, which as a
final effect leads to peritoneal fibroneogenesis. Primary
idiopathic abdominal cocoon is rare and has been mainly described
in young girls from tropical regions.11 Retrograde menstruation
causing peritoneal irritation has been speculated as the possible
cause in these cases. In a recent literature review, only four
idiopathic cases in males have been reported.1 Peritoneal
encapsulation may have a similar appearance to abdominal cocoon on
radiologic studies. This is a congenital condition in which all or
part of the small bowel is encased by an accessory peritoneal
membrane. Usually, this is asymptomatic, but has been reported to
cause bowel obstruction in a few cases. Pathologically, the
encasing membrane is normal peritoneum rather than the thick
fibrous-collagenous tissue seen in abdominal cocoon.12 CONCLUSION
Although abdominal cocoon is an unusual cause of small bowel
obstruction, it can be diagnosed preoperatively as it may have a
distinct appearance on CT of clumped bowel loops encased by a thick
membrane. It most commonly occurs in patients on CAPD or in
adolescent girls in the tropics, but rarely can occur in the
absence of medical or surgical risk factors, as in this case.
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