lymphangioma/غثيان

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Lymphangioma of the ileum causing acute abdominal pain in an adult, a very rare finding during surgery; Case report with literature review.

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Lymphangioma of the gastrointestinal tract is very rare, 75 % of the lesions affect the neck and 20 % affect the axillary region, the rest are seen in the mediastinum, the visceral organs, the retroperitoneum, the mesentery, or in the bones. Lymphangioma of the gastrointestinal tract

Pediatric abdominal lymphangiomas: a plea for early recognition.

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Abdominal lymphangiomas are usually classified together with mesenteric cysts. However, they differ by location, histology, and potential for recurrence, and should be considered a separate clinical entity. Thirteen children, aged 2 weeks to 11 years (mean, 5.8 years), with abdominal lymphangiomas

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

New Approach to Rare Pediatric Multicystic Mesenteric Lymphangioma; Would It Guide the Development of Targeted Therapy?

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In children, lymphangiomas are extremely rare pathologic entities that are characterized by unusual locations. The mesenteric localization is extremely rare in children, and the clinical signs usually mimic an acute abdominal syndrome. For most of the cases, their diagnosis is established by the

Peripancreatic cystic lymphangioma diagnosed by endoscopic ultrasound/fine-needle aspiration: a rare mesenchymal tumour.

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A 73-year-old man presented with a 5-month history of intermittent nausea, vomiting, central abdominal discomfort and a 17-pound weight loss over the past year. Laboratory testing, including a complete blood count with differential, liver function testing, amylase and lipase studies were normal. A

Mesenteric cystic lymphangioma mimicking malignancy.

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Mesenteric cystic lymphangiomas are benign tumours arising from the mesentery, and have no known aetiology. Patients might be discovered incidentally to have asymptomatic mesenteric cysts, or they can present with symptoms such as pain, nausea and vomiting. A 27-year-old man presented with vague

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

Gastric lymphangioma.

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Gastric lymphangioma is a rare benign gastric tumor composed of unilocular or multilocular lymphatic spaces. On gastrofiberscopy a submucosal tumor covered with smooth transparent normal mucosa is revealed in the stomach with or without a stalk. Endoscopic ultrasonography has become an indispensable

Pancreatic cystic lymphangioma: diagnostic approach with MDCT and MR imaging.

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Lymphangiomas are rare congenital benign tumors arising from the lymphatic system mostly encountered in the neck and axillary regions of pediatric patients. Pancreatic cystic lymphangiomas very rarely occur in adults. Radiologically, the lesion may mimic pancreatic carcinoma and should be considered

Splenic lymphangioma that manifested as a solid-cystic mass: a case report.

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Lymphangioma, a congenital malformation of the lymphatic system, is usually found in children, and generally occurs in the neck and mediastinum. It is rarely found in the spleen. The clinical features of splenic lymphangioma typically include abdominal pain, nausea, and abdominal distention.

Laparoscopic splenectomy for adult lymphangiomas of the spleen: case series and review of literature.

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OBJECTIVE Spleen lymphangiomas are rare congenital malformations of the lymphatics. There is a paucity of data in the literature on the evaluation and laparoscopic treatment for adult spleen lymphangiomas. The aim of this study is to further elucidate the feature of this tumor and laparoscopic

Mesenteric lymphangioma causing bowel obstruction: report of one case.

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A 6-year-old female was sent to our ER due to nausea, vomiting and abdominal distension for 2 days. This child had a history of constipation and failed intermittent medical treatment for 2 years. Her plain abdominal X-ray showed multiple intestinal loops and under the impression of acute abdomen

[Cystic lymphangioma of the mesentery. Clinical, radiological, and morphological analysis].

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BACKGROUND The cystic mesenteric lymphangioma is a rare benign neoplasia, that can be misdiagnosed with others cystic intra-abdominal tumors. OBJECTIVE To shown the clinical and histopathological features of a cystic mesenteric lymphangioma. METHODS A 17-year old male with a past history of 17 days

Small bowel lymphangioma causing ileo-ileal intussusception in adults.

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UNASSIGNED Lymphangioma is a rare benign tumor found in gastrointestinal tract. Most lymphangiomas can occur at any age and but mostly are found in children and infants. They are mainly due to malformation of the lymphatic system. They occur mainly in the head, neck and oral cavity, but less

Splenic lymphangioma in adulthood: A case report.

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Splenic disease are uncommon and primary tumors of the spleen are very rare. These are classified as splenic cyst, benign and malignant tumors. Splenic lymphangioma is a rare, slow-growing benign tumor of the spleen. More often seen in children, it is a congenital malformation of the

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