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Journals / Turkish Journal of Pediatrics / 2015 / Cilt: 57 - Sayı: 1

Angiomatoid fibrous histiocytoma: case report and review of the literature

Canten TATAROĞLU
NİL ÇULHACI
Emre ÇEÇEN
Pages
102–104
DOI
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⚡ TL;DR(Too Long; Didn't Read)

Herein, we present a case of angiomatoid fibrous histiocytoma with systemic symptoms before any mass was clinically detectable, arising in the scalp of a 10-year-old girl

📌 3 Key Takeaways

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Objective & Hypothesis:Tataroğlu C, Çulhacı N, Çeçen E.
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Key Findings & Data:Turk J Pediatr 2015; 57: 102-104.Angiomatoid fibrous histiocytoma is a rare soft tissue tumor of uncertain differentiation and low metastatic potential, which occurs predominantly in children and young adults.
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Conclusion & Impact:Herein, we present a case of angiomatoid fibrous histiocytoma with systemic symptoms before any mass was clinically detectable, arising in the scalp of a 10-year-old girl
🔬Design:Review & Systematic Survey
📍Scope:2015 Verileri
⚙️Variables:Domain Parameters

Özet

Tataroğlu C, Çulhacı N, Çeçen E. Angiomatoid fibrous histiocytoma: case report and review of the literature. Turk J Pediatr 2015; 57: 102-104.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, sheets of dendritic-like tumor cells with bland nuclei and blood-filled cystic cavities. Herein, we present a case of angiomatoid fibrous histiocytoma with systemic symptoms before any mass was clinically detectable, arising in the scalp of a 10-year-old girl

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Cite This Article

TATAROĞLU, C., ÇULHACI, N., ÇEÇEN, E. (2015). Angiomatoid fibrous histiocytoma: case report and review of the literature. Turkish Journal of Pediatrics, Cilt: 57 - Sayı: 1, 102–104. https://ajindex.com/articles/412274

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