Intranodal Palisaded Myofibroblastoma; a Case Report and Review of the Literature

被引:7
作者
Koseoglu, R. Dogan [1 ]
Ozkan, Namik [2 ]
Filiz, Nurper Onuk [1 ]
Kayaoglu, H. Ayhan [2 ]
Aydin, Mehtap [3 ]
Culha, Emre N. [4 ]
Ersoy, Omer F. [2 ]
机构
[1] Gaziosmanpasa Univ, Dept Pathol, Sch Med, TR-60030 Tokat, Turkey
[2] Gaziosmanpasa Univ, Dept Gen Surg, Sch Med, TR-60030 Tokat, Turkey
[3] Ankara Med Res & Training Hosp, Dept Pathol, Ankara, Turkey
[4] State Hosp Sincan, Pathol Lab, Ankara, Turkey
关键词
Myofibroblastoma; Intranodal palisaded myofibroblastoma; Amianthoid fiber; SPINDLE-CELL TUMOR; METAPLASTIC BONE-FORMATION; AMIANTHOID FIBERS; LYMPH-NODE; KAPOSIS-SARCOMA; REGION;
D O I
10.1007/s12253-008-9122-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Intranodal palisaded myofibroblastoma (IPM) also called as intranodal hemorrhagic spindle cell tumor with amianthoid fibers is a distinctive and rare mesenchymal neoplasm of lymph nodes. This entity generally misdiagnosed as intranodal Kaposi's sarcoma or schwannoma in past. In contrast to Kaposi's sarcoma, it behaves in a benign fashion and does not need any further therapy except total surgical resection of the mass. This neoplasm has a great predilection for the inguinal region. The lesion presents typically as a unilateral, painless, solitary mass. To our knowledge, approximately 53 cases of IPM have been reported in the English-language literature. We present a 43-year-old-male patient with IPM and discuss histological, immunohistochemical features and pathogenesis of this rare benign neoplasm.
引用
收藏
页码:297 / 300
页数:4
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