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

被引:5
|
作者
Sun, Yuefang [1 ]
Zhao, Ming [2 ]
Lao, I. Weng [3 ,4 ]
Yu, Lin [3 ,4 ]
Wang, Jian [3 ,4 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Dept Pathol, Peoples Hosp 10, 301 Yanchang Middle Rd, Shanghai 200072, Peoples R China
[2] Zhejiang Prov Peoples Hosp, Dept Pathol, Hangzhou 310014, Zhejiang, Peoples R China
[3] Fudan Univ, Dept Pathol, Shanghai Canc Ctr, Shanghai 200032, Peoples R China
[4] Fudan Univ, Dept Oncol, Shanghai Med Coll, 270 Dong An St, Shanghai 200032, Peoples R China
关键词
Hemangioendothelioma; Pseudomyogenic hemangioendothelioma; FOSB; SARCOMA-LIKE HEMANGIOENDOTHELIOMA; EPITHELIOID SARCOMA; FOSB; FUSION; BONE; TUMOR;
D O I
10.1007/s00428-020-02753-4
中图分类号
R36 [病理学];
学科分类号
100104 ;
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 1064 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:10
相关论文
共 50 条
  • [1] The clinicopathological spectrum of pseudomyogenic hemangioendothelioma: report of an additional series with review of the literature
    Yuefang Sun
    Ming Zhao
    I Weng Lao
    Lin Yu
    Jian Wang
    [J]. Virchows Archiv, 2020, 477 : 231 - 240
  • [2] Pseudomyogenic Hemangioendothelioma: Case Report and Review of the Literature
    Raftopoulos, Emily
    Royer, Michael
    Warren, Mildred
    Zhao, Jin
    Rush, Walter
    [J]. AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2018, 40 (08) : 597 - 601
  • [3] Oral Pseudomyogenic Hemangioendothelioma: Case Report and Review of the Literature
    Austin J. Shackelford
    Carleigh R. Canterbury
    Michael A. Perrino
    Joseph Wang
    Elizabeth M. Philipone
    Scott M. Peters
    [J]. Head and Neck Pathology, 2020, 14 : 1134 - 1138
  • [4] Oral Pseudomyogenic Hemangioendothelioma: Case Report and Review of the Literature
    Shackelford, Austin J.
    Canterbury, Carleigh R.
    Perrino, Michael A.
    Wang, Joseph
    Philipone, Elizabeth M.
    Peters, Scott M.
    [J]. HEAD & NECK PATHOLOGY, 2020, 14 (04): : 1134 - 1138
  • [5] The clinicopathological spectrum of sclerosing epithelioid fibrosarcoma: report of an additional series with review of the literature
    Peng, Yan
    Zhang, Dachuan
    Lei, Ting
    Xie, Jun
    Wu, Chao
    Wang, Hui
    Shi, Yongqiang
    Li, Qing
    Wang, Jian
    [J]. PATHOLOGY, 2023, 55 (03) : 355 - 361
  • [6] The management of pseudomyogenic hemangioendothelioma of the foot: A case report and review of the literature
    Pranteda, Guglielmo
    Magri, Francesca
    Muscianese, Marta
    Pigliacelli, Flavia
    D'Arino, Andrea
    Federico, Alessandro
    Pranteda, Giulia
    Bartolazzi, Armando
    [J]. DERMATOLOGIC THERAPY, 2018, 31 (06)
  • [7] Primary pseudomyogenic hemangioendothelioma of bone: case report and review of the literature
    Squillaci, S.
    Pitino, A.
    Spairani, C.
    Rassu, P. C.
    Chiapuzzo, E.
    Kutzner, H.
    [J]. PATHOLOGICA, 2018, 110 (02) : 96 - 101
  • [8] Clinicopathological study of pseudomyogenic hemangioendothelioma
    Yang, Ningning
    Huang, Yuchen
    Yang, Panpan
    Yan, Wentian
    Zhang, Shan
    Li, Nan
    Feng, Zhenzhong
    [J]. DIAGNOSTIC PATHOLOGY, 2023, 18 (01) : 25
  • [9] Clinicopathological study of pseudomyogenic hemangioendothelioma
    Ningning Yang
    Yuchen Huang
    Panpan Yang
    Wentian Yan
    Shan Zhang
    Nan Li
    Zhenzhong Feng
    [J]. Diagnostic Pathology, 18
  • [10] Pseudomyogenic Hemangioendothelioma: Report of an Additional Case With Aggressive Clinical Course
    Sheng, Weiqi
    Pan, Yuncui
    Wang, Jian
    [J]. AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2013, 35 (05) : 597 - 600