lymphangioma/diarreia

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Lymphangioma of the gallbladder in adults: review of the literature and a case report.

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BACKGROUND Lymphangiomas of the gallbladder in adults are extremely rare with only 10 cases published worldwide to date. METHODS We herein report a case of a 26-year-old male who presented with abdominal right upper quadrant pain, nausea, vomiting, and diarrhea. An ultrasound, computer tomography

Retroperitoneal cystic lymphangioma in an adult: A case report and review of the literature.

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Lymphangiomas are rare benign cystic tumors of the lymphatic system. Retroperitoneal lymphangiomas account for 1% of all lymphangiomas, and approximately 186 cases have been reported. They may clinically present as a palpable abdominal mass and can cause diagnostic dilemmas with other

Adult intussusception secondary to lymphangioma of the cecum: a case report.

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We report the case of a patient with ileocolic intussusception caused by cecal lymphangioma. A 45-year-old man visited our hospital with a 2-month history of frequent episodes of watery diarrhea (>/= 5 times/day) and intermittent abdominal pain. A cecal submucosal tumor with mucosal ulceration and

Cystic lymphangioma of the colon. Endoscopic and histologic features.

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Cystic lymphangiomas are rare benign tumors of the gastrointestinal tract. Such a lesion was found in the colon of a man who presented with diarrhea and rectal bleeding. The colonoscopic appearances of a smooth, soft polypoid lesion on a broad base should alert the clinician to suspect such a

[Pneumatosis coli vs. deep cystic colitis].

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We present the case of a 63-year-old female who with no previous history presented with episodes of self-limited diarrhea without fever, general repercussions, abnormal elements or tenesmus. Biochemistry: no abnormality. Parasite and feces culture: negative. Colonoscopy: at 20 to 40 cm from the anal

Intra-Abdominal Lymphangiomatosis with Bone Marrow Involvement in a 7-Year Old Girl: A Case Report.

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Lymphangiomas are rare tumors. When they occur at different locations, they are referred to as lymphangiomatosis. Here we describe a case of lymphangiomatosis presenting with chronic diarrhea and failure to thrive. Etiology, clinical presentations and treatment options will be discussed.

Laparoscopic resection of a lymphangiomatous cyst of the colon: a case report.

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BACKGROUND Lymphangiomatous cysts are submucosal masses that are rarely found in the gastrointestinal tract and more often in the neck, oral cavity, and skin. These cysts are benign tumors and mostly clinically silent. Symptoms include abdominal pain, diarrhea, and rectal bleeding. Their

Holmes-Adie syndrome, autoimmune hepatitis and celiac disease: a case report.

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A 35-year-old female patient presented with the following symptoms of Holmes-Adie syndrome: photophobia,enlargement of the left pupil unresponsive to light, Achilles areflexia. The pilocarpine test was positive. No tumor or other neurological abnormality was found. She had a 19-year history of

Diagnosis and outcome of small bowel tumors found by capsule endoscopy: a three-center Australian experience.

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OBJECTIVE The objective of the study was to examine diagnosis and outcome in a series of patients with small bowel tumors detected by capsule endoscopy (CE) in three Australian centers. METHODS Review of prospectively collected data from 416 CEs identified 27 tumors in 26 patients. Clinical

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