2008
DOI: 10.1007/s11605-007-0441-3
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Intraabdominal Schwannomas: A Single Institution Experience

Abstract: Intraabdominal schwannomas are rare tumors, which are most frequently located within the GIT. GIT schwannomas are difficult if not impossible to diagnose preoperatively as endoscopic and radiologic findings are nonspecific. The treatment of choice is complete surgical excision because of diagnostic uncertainty, and the long-term outcome is excellent as these lesions are uniformly benign.

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Cited by 36 publications
(62 citation statements)
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“…They are frequently surrounded by a cuff of lymphoid aggregates, highly cellular, and composed mainly of bipolar spindle cells. Verocay bodies, vascular hyalinization, Antoni A and B areas, and a typical palisading structure are typically absent, unlike in conventional schwannomas (4,8). On the other hand, the lesser sac schwannoma demonstrates the typical pathologic features of peripheral and soft tissue.…”
Section: Discussionmentioning
confidence: 95%
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“…They are frequently surrounded by a cuff of lymphoid aggregates, highly cellular, and composed mainly of bipolar spindle cells. Verocay bodies, vascular hyalinization, Antoni A and B areas, and a typical palisading structure are typically absent, unlike in conventional schwannomas (4,8). On the other hand, the lesser sac schwannoma demonstrates the typical pathologic features of peripheral and soft tissue.…”
Section: Discussionmentioning
confidence: 95%
“…Because of its rarity, it is not diagnosed preoperatively. The most common presenting symptom is an episode of intermittent GIT blee- ding, abdominal pain, epigastric discomfort and bloatedness, epigastric mass, and rarely, obstruction (4,7). In this patient, the pylorus was covered with normal mucosal epithelium without ulceration but obstruction may have been the result of the secondary effect of the 5 mm PS.…”
Section: Discussionmentioning
confidence: 99%
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“…They commonly originate in the stomach [3]- [5] and rarely present in large bowel. In large bowel, the commonest location being the caecum and rectosigmoid colon [6] but rare in ascending colon [7]- [9].…”
Section: Discussionmentioning
confidence: 99%