An unusual histopathologic feature of angiomatoid fibrous histiocytoma – A case report and molecular study

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Angiomatoid fibrous histiocytoma: case report and review of the literature.

Angiomatoid fibrous histiocytoma is a rare soft tissue tumor of uncertain differentiation and low metastatic potential, which occurs predominantly in children and young adults. It occurs mostly within the extremities, trunk, head and neck. It can be associated with systemic manifestations such as anemia, pyrexia and malaise. Its morphology is distinct, with an outer shell of lymphoid tissue, sh...

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Cervical Angiomatoid Fibrous Histiocytoma

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A case of aneurysmal ("angiomatoid") fibrous histiocytoma (AFH) in a 12-year-old girl is presented with its unusual clinicopathologic features. The lesion had the full microscopic characteristics of AFH described in prior reports, but it also had some features that differed from the original description of the disorder, such as the involvement of subcutis, its occurrence in the scalp, and a doc...

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Malignant Fibrous Histiocytoma of the Lung: A Case Report

Malignant Fibrous Histiocytoma (MFH) is the most common soft-tissue sarcoma which predominantly surfaces in the retro-peritoneum and extremity. MFH of lung is a very rare condition. The diagnosis is essentially through histologic examination. However, the invasion of the chest wall or other organs might help establish the malignant nature.We report a case of a 77-year-old man who had been prese...

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Retroperitoneal angiomatoid fibrous histiocytoma: A case report and review of the literature

Angiomatoid fibrous histiocytoma (AFH) is a rare, low-grade malignant potential soft tissue tumor which occurs most commonly in children and young adults. Only a few case reports have been described that typically occur in the extremities of the deep dermis and subcutaneous tissue, followed by the trunk, as well as the head and neck. A case report of retroperitoneal AFH is described. This prese...

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ژورنال

عنوان ژورنال: Dermatologica Sinica

سال: 2018

ISSN: 1027-8117

DOI: 10.1016/j.dsi.2018.06.004