Solitary Fibrous Tumor of the Central Nervous System: A Report of Two Cases with Emphasis on Diagnostic Pitfalls

被引:1
|
作者
Mwazha, Absalom [1 ,2 ]
Moyeni, Nondabula [3 ,4 ]
Zikalala, Zuzile [5 ,6 ]
Nhlonzi, Gamalenkosi Bonginkosi [2 ,7 ]
Baeesa, Saleh
机构
[1] Natl Hlth Lab Serv, Dept Anat Pathol, Durban, South Africa
[2] Univ KwaZulu Natal, Dept Anat Pathol, Durban, South Africa
[3] Inkosi Albert Luthuli Cent Hosp, Dept Neurosurg, Durban, South Africa
[4] Univ Kwazulu Natal, Discipline Pediat & Child Hlth, Durban, South Africa
[5] Univ KwaZulu Natal, Dr Pixley Ka Isaka Seme Mem Hosp, Dept Orthopaed Surg, 310 Bhejane St, ZA-4360 Durban, South Africa
[6] Univ KwaZulu Natal, Discipline Radiol, Durban, South Africa
[7] Ampath Pathol Labs, Dept Histopathol, Pietermaritzburg, South Africa
关键词
MENINGEAL HEMANGIOPERICYTOMA; FEATURES; MENINGIOMA; DISTINCT; SARCOMA; MR;
D O I
10.1155/2024/3467025
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Solitary fibrous tumor (SFT) is a rare primary central nervous system neoplasm that usually presents as a dural-based mass. Awareness of the entity is limited by the rarity of the tumor which renders it prone to misdiagnosis. We present two cases of SFT located in the right parafalx and intraventricular region. The cases were classified as WHO grade 1 and grade 2, respectively. The present study discusses the radiological, histomorphological, and immunohistochemical features of SFT, with emphasis on potential diagnostic pitfalls that may lead to erroneous diagnosis.
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收藏
页数:8
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