Journals / Erciyes Tıp Dergisi / 2014 / Cilt: 36 - Sayı: 4

Yüzeyel akral fibromiksoma

Superfcial acral fibromyxoma

Pages
181–183
Publication Date
2022-10-17
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In the treatment of thesetumors, complete excision is recommended because of the potential recurrence.

📌 3 Key Takeaways

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Objective & Hypothesis:Superfcial acral fbromyxoma (digital fbromyxoma) is a rare tumor with a predilection for the subungual or periungual regions ofthe hands and feet.
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Key Findings & Data:Tumor cells are often positive for CD34, CD99, and EMA immunohistochemically.
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Conclusion & Impact:In the treatment of thesetumors, complete excision is recommended because of the potential recurrence.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Superfcial acral fbromyxoma (digital fbromyxoma) is a rare tumor with a predilection for the subungual or periungual regions ofthe hands and feet. Generally, it states at dermis and has no capsule. Proliferation of the spindle and stellate-shaped fbroblasticcells in storiform and a scattered or fascicular pattern are characteristic features of this tumor. There are mast cells in myxoid orcollagenous stroma. Tumor cells are often positive for CD34, CD99, and EMA immunohistochemically. In the treatment of thesetumors, complete excision is recommended because of the potential recurrence. Here, we present a 60-year-old male patientwith a papillomatous lesion on the second fnger of his right hand. The tumor was extending into the nail bed. After excision, itwas diagnosed as superfcial acral fbromyxoma. The histopathological and immunohistochemical features of these rare tumorsare discussed.

Özet

Yüzeyel akral fibromiksoma (dijital fibromiksoma) el ve ayakların subungual veya periungual bölgelerini tercih eden nadir bir tümördür. Genellikle, dermiste yerleşir ve kapsülü yoktur. İğcik ve yıldız şeklindeki fibroblastik hücrelerin iğ biçiminde ve dağınık veya fasiküler paternde çoğalması bu tümörün karakteristik özellikleridir. Mikzoid veya kollajen stromada mast hücreleri vardır. Tümör hücreleri immünohistokimyasal olarak CD34, CD99 ve EMA için sıklıkla pozitiftir. Bu tümörlerin tedavisinde, potansiyel rekürrens nedeniyle tam eksizyon tavsiye edilmektedir. Burada, sağ elinin ikinci parmağında bir papillomatöz lezyonu olan 60 yaşındaki erkek hasta sunulmaktadır. Tümör tırnak yatağı içine uzanmaktaydı. Eksizyondan sonra, yüzeyel akral fibromiksoma olarak tanı konuldu. Bu nadir tümörlerin histopatolojik ve immünohistokimyasal özellikleri tartışılmıştır.

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Cite This Article

KARABAĞLI, Y., CANAZ, F., ARIK, D. (2022). Yüzeyel akral fibromiksoma. Erciyes Tıp Dergisi, Cilt: 36 - Sayı: 4, 181–183. https://ajindex.com/articles/502350

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References (1)

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