Langerhans cell sarcoma arising from antecedent langerhans cell histiocytosis: A case report

被引:16
作者
Yi, Wu [1 ]
Chen, Wan-yuan [2 ]
Yang, Tian-xin [1 ]
Lan, Jian-ping [1 ]
Liang, Wen-na [3 ]
机构
[1] Hangzhou Med Coll, Peoples Hosp, Zhejiang Prov Peoples Hosp, Dept Haematol, Hangzhou, Zhejiang, Peoples R China
[2] Hangzhou Med Coll, Peoples Hosp, Zhejiang Prov Peoples Hosp, Dept Pathol, Hangzhou, Zhejiang, Peoples R China
[3] Hangzhou Med Coll, Peoples Hosp, Zhejiang Prov Peoples Hosp, Dept Nephrol, Hangzhou 310000, Zhejiang, Peoples R China
关键词
chemotherapy; langerhans cell sarcoma; surgical resection; LYMPH-NODE; NEOPLASM;
D O I
10.1097/MD.0000000000014531
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale:Langerhans cell sarcoma (LCS) is a rare, high-grade neoplasm characterized by overtly malignant cytologic features and a poor prognosis. Herein, we present a rare case of langerhans cell histiocytosis (LCH) that later transformed into langerhans cell sarcoma 11 months after the benign mass was excised from soft tissue in the right groin.Patient concerns:A 41-year-old patient who presented with a mass in the right groin for 3 years earlier after being bitten by ants.Diagnoses:The patient was diagnosed with langerhans cell sarcoma arising from antecedent langerhans cell histiocytosis.Interventions:The patient underwent with 6 cycles of a modified etoposide, cyclophosphamide, vindesine, dexamethasone (E-CHOP) regimen.Outcomes:The patient is currently receiving follow-up care.Lessons:LCH transformed into LCS is a rare case. E-CHOP as an effective first-line therapy to treat LCS cases, but, the mechanism is unclear. Due to their rarity, further data on clinical outcomes are necessary to establish the optimal treatment strategy for LCS.
引用
收藏
页数:4
相关论文
共 17 条
  • [1] Cutaneous langerhans cell sarcoma:: A case report and review of the literature
    Bohn, Olga L.
    Ruiz-Argueelles, Guillermo
    Navarro, Leticia
    Saldivar, Jesus
    Sanchez-Sosa, Sergio
    [J]. INTERNATIONAL JOURNAL OF HEMATOLOGY, 2007, 85 (02) : 116 - 120
  • [2] BONETTI F, 1985, CANCER-AM CANCER SOC, V55, P2417, DOI 10.1002/1097-0142(19850515)55:10<2417::AID-CNCR2820551020>3.0.CO
  • [3] 2-9
  • [4] Langerhans Cell Sarcoma of the Axillary Lymph Node: A Case Report and Review of the Literature
    Calli, Aylin Orgen
    Morgul, Yelda
    Alacacioglu, Inci
    Bener, Sadi
    Payzin, Bahriye
    [J]. TURKISH JOURNAL OF HEMATOLOGY, 2013, 30 (02) : 198 - 203
  • [5] TRUE HISTIOCYTIC NEOPLASM OF LANGERHANS CELL TYPE
    DELABIE, J
    DEWOLFPEETERS, C
    DEVOS, R
    VANDENBERGHE, E
    KENNES, K
    DEJONGE, I
    DESMET, V
    [J]. JOURNAL OF PATHOLOGY, 1991, 163 (03) : 217 - 223
  • [6] Langerhans Cell. Sarcoma in Two Young Children: Imaging Findings on Initial. Presentation and Recurrence
    Do Chung, Woong
    Im, Soo Ah
    Chung, Nak Gyun
    Park, Gyeong Sin
    [J]. KOREAN JOURNAL OF RADIOLOGY, 2013, 14 (03) : 520 - 524
  • [7] Langerhans cell sarcoma
    Ferringer, Tammie
    Banks, Peter M.
    Metcalf, John S.
    [J]. AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2006, 28 (01) : 36 - 39
  • [8] Jaffe ES, 2001, WHO CLASSIFICATION T
  • [9] Pulmonary manifestation of a Langerhans cell sarcoma:: case report and review of the literature
    Jülg, BD
    Weidner, S
    Mayr, D
    [J]. VIRCHOWS ARCHIV, 2006, 448 (03) : 369 - 374
  • [10] Langerhans cell sarcoma of the nasopharynx: a rare case
    Keklik, M.
    Sivgin, S.
    Kontas, O.
    Abdulrezzak, U.
    Kaynar, L.
    Cetin, M.
    [J]. SCOTTISH MEDICAL JOURNAL, 2013, 58 (04) : E17 - E20