Literature DB >> 16519396

Angiomatoid fibrous histiocytoma with pain in a child.

Piriya Sutthiruangwong1, Voranuch Thanakit, Apichat Assavamongkolkul.   

Abstract

Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor with low-grade malignancy which occurs chiefly in children and young adults. Mostly, the tumor develops in the extremities or the trunk. The tumor has a relatively rare metastasis and its overall clinical outcome is excellent. The authors present a case of AFH of the subcutis on a left elbow of an 11-year-old boy. Clinically, the tumor appears as a cutaneous nodule with slow growth. Pain and adjacent lymphadenopathy are leading symptoms of the patient. Histological examination shows the classical morphological features of AFH with focal cellular atypia. The tumor has immunoreactivity to vimentin and CD68 but negative to CD34, desmin, CD117 and S-100 protein. Because of its rarity, we report a case with an uncommon clinical presentation in a Thai patient.

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Year:  2005        PMID: 16519396

Source DB:  PubMed          Journal:  J Med Assoc Thai        ISSN: 0125-2208


  2 in total

1.  Angiomatoid fibrous histiocytoma: novel MR imaging findings.

Authors:  Salutario J Martinez; Courtney Coursey Moreno; Emily N Vinson; Leslie G Dodd; Brian E Brigman
Journal:  Skeletal Radiol       Date:  2016-02-27       Impact factor: 2.199

2.  Angiomatoid fibrous histiocytoma (AFH) unusual clinical presentation and unique radiological findings.

Authors:  Mohammed Khader; Tahiya Alyafei; Sulafa Ibrahim; Orwa Elaiwy
Journal:  BJR Case Rep       Date:  2020-12-02
  2 in total

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