Primary pseudomyogenic haemangioendothelioma of bone

被引:35
作者
Sheng, W. Q. [2 ]
Wang, J. [1 ,2 ]
机构
[1] Fudan Univ, Dept Pathol, Inst Canc Res, Canc Hosp, Shanghai 200032, Peoples R China
[2] Fudan Univ, Dept Oncol, Shanghai Med Coll, Shanghai 200032, Peoples R China
关键词
bone; epithelioid sarcoma; haemangioendothelioma; immunohistochemistry; SARCOMA-LIKE HEMANGIOENDOTHELIOMA; FIBROMA-LIKE VARIANT; EPITHELIOID SARCOMA; INDOLENT BEHAVIOR; TUMORS;
D O I
10.1111/j.1365-2559.2012.04347.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sheng W Q & Wang J ?(2012) Histopathology?Primary pseudomyogenic haemangioendothelioma of bone Aims: Pseudomyogenic haemangioendothelioma is a recently described vascular neoplasm that occurs most commonly in the soft tissue of distal extremities of young adults. Occurrence outside the somatic soft tissue has not been described thus far. We present here a unique case of pseudomyogenic haemangioendothelioma that arose in the long tubular bones of the lower extremity. Methods and results: The initial open biopsy was interpreted as a fibrous histiocytoma. However, the curettage specimen showed prominent epithelioid cytomorphology with a striking rhabdomyoblast-like appearance. By immunohistochemistry, the linear membranous staining of CD31 was highly suggestive of endothelial differentiation of the tumour cells. Conclusions: To the best of our knowledge, this case represents the first example of primary pseudomyogenic haemangioendothelioma of bone. Clinical and pathological correlation with application of immunohistochemistry is mandatory in establishing the correct diagnosis and excluding tumours with overlapping features.
引用
收藏
页码:1219 / 1224
页数:6
相关论文
共 17 条
[1]   Epithelioid sarcoma-like hemangioendothelioma [J].
Billings, SD ;
Folpe, AL ;
Weiss, SW .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2003, 27 (01) :48-57
[2]  
Billings SD, 2011, AM J SURG PATHOL, V35, P1088, DOI 10.1097/PAS.0b013e31821caf1c
[3]   PRIMARY VASCULAR TUMORS OF LYMPH-NODES OTHER THAN KAPOSIS-SARCOMA - ANALYSIS OF 39 CASES AND DELINEATION OF 2 NEW ENTITIES [J].
CHAN, JKC ;
FRIZZERA, G ;
FLETCHER, CDM ;
ROSAI, J .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1992, 16 (04) :335-350
[4]   Epithelioid angiosarcoma of the bone - A series of 10 cases [J].
Deshpande, V ;
Rosenberg, AE ;
O'Connell, JX ;
Nielsen, GP .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2003, 27 (06) :709-716
[5]  
Fletcher C DM., 2002, World Health Organisation Classification of tumours: Tumours of Soft Tissue and Bone, V3rd
[6]  
Hornick JL, 2008, MODERN PATHOL, V21, p13A
[7]   Pseudomyogenic Hemangioendothelioma: A Distinctive, Often Multicentric Tumor With Indolent Behavior [J].
Hornick, Jason L. ;
Fletcher, Christopher D. M. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2011, 35 (02) :190-201
[8]   Loss of INI1 Expression is Characteristic of Both Conventional and Proximal-type Epithelioid Sarcoma [J].
Hornick, Jason L. ;
Dal Cin, Paola ;
Fletcher, Christopher D. M. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2009, 33 (04) :542-550
[9]   Epithelioid hemangioendothelioma of bone [J].
Kleer, CC ;
Unni, KK ;
McLeod, RA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1996, 20 (11) :1301-1311
[10]   Epithelioid sarcoma: An immunohistochemical analysis of 112 classical and variant cases and a discussion of the differential diagnosis [J].
Miettinen, M ;
Fanburg-Smith, JC ;
Virolainen, M ;
Shmookler, BM ;
Fetsch, JF .
HUMAN PATHOLOGY, 1999, 30 (08) :934-942