Angiographic and pathologic features of probable primary carcinoid-like hepatic tumors

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Pathologic and Radiologic Features of Primary Bone Tumors.

Accurate diagnosis of primary bone tumors requires evaluation of clinical, radiologic, and pathologic features. Thus, communication among the orthopedic surgeon, the radiologist, and the pathologist is necessary to avoid serious diagnostic errors and subsequent therapeutic mismanagement. The following clinical parameters provide essential diagnostic information and should be part of every diagn...

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Primary hepatic carcinoid tumor.

OBJECTIVES To describe a rare case of primary carcinoid tumor of the liver and its management. CLINICAL PRESENTATION AND INTERVENTIONS A 44-year-old Nigerian male presented with a big inoperable liver mass, which proved to be a carcinoid tumor by fine needle aspiration cytology. Extensive search for a primary lesion including laparotomy and peroperative ultrasound failed to find a primary les...

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Primary hepatic carcinoid tumor

Primary hepatic carcinoid tumor is rare and poses a challenge for diagnosis and management. We presented a case of primary hepatic carcinoid tumor in a 53-year-old female with a complaint of right upper abdominal pain. Computer tomography scans revealed a hypervascular mass in segment 4 of the liver. An ultrasonography-guided biopsy showed a carcinoid tumor. No other lesions were found by the r...

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Primary carcinoid tumors of the liver

A primary hepatic tumor with histologic features suggestive of carcinoid tumor is reported, and six previously reported cases reviewed. Tumor cells contained electron dense secretory granules with an average diameter 150-200 nm which demonstrated positive argyrophilic reactions. On immunohistochemistry, chromogranin A was positively stained. No endocrine syndrome was present and an alternative ...

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Primary Hepatic Carcinoid Tumor with Poor Outcome.

Primary Hepatic Carcinoid Tumor (PHCT) represents an extremely rare clinical entity with only a few cases reported to date. These tumors are rarely associated with metastasis and surgical resection is usually curative. Herein, we report two cases of PHCT associated with poor outcomes due to late diagnosis. Both cases presented late with non-specific symptoms. One patient presented after a 2-wee...

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ژورنال

عنوان ژورنال: Gastrointestinal Radiology

سال: 1978

ISSN: 0364-2356,1432-0509

DOI: 10.1007/bf01887101