The clinicopathological spectrum of pseudomyogenic hemangioendothelioma: report of an additional series with review of the literature

被引:0
作者
Yuefang Sun
Ming Zhao
I Weng Lao
Lin Yu
Jian Wang
机构
[1] Shanghai Tenth People’s Hospital,Department of Pathology
[2] Tenth People’s Hospital of Tongji University,Department of Pathology
[3] Zhejiang Provincial People’s Hospital,Department of Pathology
[4] Fudan University Shanghai Cancer Center,Department of Oncology Shanghai Medical College
[5] Fudan University,undefined
来源
Virchows Archiv | 2020年 / 477卷
关键词
Hemangioendothelioma; Pseudomyogenic hemangioendothelioma; FOSB;
D O I
暂无
中图分类号
学科分类号
摘要
We present here our experience with 24 cases of pseudomyogenic hemangioendothelioma (PMHE) to further delineate its clinicopathological spectrum. There were 18 males and 6 females with a median age of 28 years (range 10~64 years). Most patients presented with erythematous nodules or papules, with or without pain. The majority (63%) occurred in the lower extremities, whereas a minority involved the trunk (25%), upper extremities (8%), and head and neck (4%). Six cases (25%) had a primary bone origin. With physical and radiological examinations, 16 cases (67%) manifested as multifocal disease, involving multiple tissue planes or different bones within the anatomic region. Six cases (25%) involved skin, soft tissue, and bone simultaneously. Histologically, all cases showed features consistent with a PMHE characterized by loose fascicles or sheets of plump spindled to epithelioid cells harboring brightly eosinophilic cytoplasm and vesicular nuclei. In addition, five cases (21%) contained a prominent myxoid matrix, and one case displayed perineural and intravascular invasion. The follow-up information available in 18 patients revealed local recurrence in 4 patients (22%) and persistent disease in 8 patients (44%), respectively. One patient developed bilateral pulmonary metastases which showed significant remission after systemic chemotherapy. None of the patients died of the disease. As the clinical appearance of PMHE can be deceptive, a radiological examination is essential in identifying an insidious multifocal disease. Although PMHE has a predilection for the distal extremities of young males, this rare tumor type could also occur in unusual sites and affect middle-aged adults of both genders. The striking myoid appearance in association with myxoid stromal change may represent a potential diagnostic pitfall. Biologically, PMHE has an indolent clinical behavior, albeit metastatic disease may occur in rare instance.
引用
收藏
页码:231 / 240
页数:9
相关论文
共 233 条
[61]  
Tsukamoto Y(undefined)undefined undefined undefined undefined-undefined
[62]  
Ito T(undefined)undefined undefined undefined undefined-undefined
[63]  
Watanabe T(undefined)undefined undefined undefined undefined-undefined
[64]  
Nakagawa N(undefined)undefined undefined undefined undefined-undefined
[65]  
Haneda T(undefined)undefined undefined undefined undefined-undefined
[66]  
Nagai M(undefined)undefined undefined undefined undefined-undefined
[67]  
Yamanishi K(undefined)undefined undefined undefined undefined-undefined
[68]  
Hirota S(undefined)undefined undefined undefined undefined-undefined
[69]  
Raftopoulos E(undefined)undefined undefined undefined undefined-undefined
[70]  
Royer M(undefined)undefined undefined undefined undefined-undefined