Unusual multifocal intraosseous papillary intralymphatic angioendothelioma (Dabska tumor) of facial bones: a case report and review of literature

被引:18
作者
Li, Bin [1 ]
Li, Yang [1 ]
Tian, Xiao-ying [2 ]
Li, Zhi [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Pathol, Guangzhou 510080, Guangdong, Peoples R China
[2] Hong Kong Baptist Univ, Sch Chinese Med, Kowloon Tong, Hong Kong, Peoples R China
关键词
Papillary intralymphatic angioendothelioma; Dabska tumor; Osteolytic lesion; Differential diagnosis; VASCULAR TUMORS; CHILDHOOD; FEATURES; SARCOMA;
D O I
10.1186/1746-1596-8-160
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Papillary intralymphatic angioendothelioma (PILA) or Dabska tumor is extremely rare, and often affects the skin and subcutaneous tissues of children. Since its first description by Dabska, only a few intraosseous cases have been described in the literature and none of them presents with multifocal osteolytic lesion of bones. We present a case of unusual multifocal intraosseous PILA in facial bones occurring in a 1 year 3 month old male child. Computed tomography (CT) scan revealed multifocal osteolytic lesions were located at the left zygoma, left orbital bone and right maxillary. Histologically, the lesions were ill-defined and composed of multiple delicate interconnecting vascular channels with papillae formation which projected into the lumen lined by atypical plumped endothelial cells. The vascular channels were also lined by plump cuboidal endothelial cells with focal hobnailed or "match-head" appearance. In some areas, endothelial cells formed solid-appearing aggregates with vessel lumens. By immunohistochemistry, the tumor cells were positive for CD31, CD34 and D2-40 at varying intensity. A final diagnosis of intraosseous PILA was made. To the best of our knowledge, this case is the first case of primary multifocal osseous PILA.
引用
收藏
页数:6
相关论文
共 22 条
[1]  
Antosz Z, 2010, NEUROENDOCRINOL LETT, V31, P454
[2]  
Bernic A, 2012, COLLEGIUM ANTROPOL, V36, P171
[3]   Dabska tumor (Endovascular papillary angioendothelioma) of testis: a case report with brief review of literature [J].
Bhatia, Alka ;
Nada, Ritambra ;
Kumar, Yashwant ;
Menon, Prema .
DIAGNOSTIC PATHOLOGY, 2006, 1 (1)
[4]  
Calonje E, 2002, WHO CLASSIFICATION T, P167
[5]  
DABSKA M, 1969, CANCER-AM CANCER SOC, V24, P503, DOI 10.1002/1097-0142(196909)24:3<503::AID-CNCR2820240311>3.0.CO
[6]  
2-L
[7]   Nodal intralymphatic papillary endothelial tumour with Dabska-like features: report of a case in two mesenteric lymph nodes [J].
de Saint-Maur, Paul Prudhomme ;
Audouin, Josee ;
Cazier, Alain ;
Le Tourneau, Agnes ;
Molina, Thierry ;
Diebold, Jacques .
HISTOPATHOLOGY, 2011, 59 (05) :1027-1029
[8]   Papillary intralymphalic angioendothelioma (PILA) - A report of twelve cases of a distinctive vascular tumor with phenotypic features of lymphatic vessels [J].
Fanburg-Smith, JC ;
Michal, M ;
Partanen, TA ;
Alitalo, K ;
Miettinen, M .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1999, 23 (09) :1004-1010
[9]  
Fanburg-Smith JC, 2013, World Health Organization classification of tumors of soft tissue and bone, P148
[10]   Vascular endothelial growth factor receptor-3 (VEGFR-3): A marker of vascular tumors with presumed lymphatic differentiation, including Kaposi's sarcoma, kaposiform and Dabska-type hemangioendotheliomas, and a subset of angiosarcomas [J].
Folpe, AL ;
Veikkola, T ;
Valtola, R ;
Weiss, SW .
MODERN PATHOLOGY, 2000, 13 (02) :180-185