Malignant fibrous histiocytoma is the
mostly encountered soft tissue sarcoma around the seventh decade of life.
Usually, it is located at lower ekstremities and deep in the muscles. It is
seen in 4 histopathological subtypes, namely storiform pleomorphic, myxoid, giant
cell and inflammatory types respectively. At this presentation, there are two
malignant fibrous histiocytoma cases, one of storiform-pleomorphic and the
other of giant cell types; the first located at the axillary region and the
second located at the upper extremity subcutaneously. The first patient is 67
years of age and the second one is 71, both being males.
Malign fibröz histiositom, yedinci
dekad civarında en sıklıkla görülen yumuşak doku sarkomudur. Genellikle alt
ekstremitelerde ve kas içerisinde derin yerleşimli olan bu tümor, 4
histopatolojik tipte görülür. (Görülme sıklığına göre, storiform-pleomorfik,
mikzoid, dev hücreli ve inflamatuvar tipler.) Bu sunumda biri aksilla, diğeri
ise üst ekstremitede subkutan yerleşimli, ilki storiform-pleomorfik, ikincisi
ise dev hücreli tipte iki malign fibröz histiositom olgusu yer almaktadır. Hastalardan
ilki 67, ikincisi ise 71 yaşında olup, her ikisi de erkektir.
Primary Language | Turkish |
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Subjects | Pathology |
Journal Section | Olgu Sunumu |
Authors | |
Publication Date | December 30, 1996 |
Submission Date | September 6, 1996 |
Published in Issue | Year 1996 Volume: 1 Issue: 2 |
The articles in the Journal of "Acta Medica Nicomedia" are open access articles licensed under a Creative Commons Attribution-ShareAlike 4.0 International License at the web address https://dergipark.org.tr/tr/pub/actamednicomedia