Malignant Extrarenal Rhabdoid tumor derived from the greater omentum: A case report and literature review

被引：0

作者：

Shao, Xue ^{[1
,2
]}

Liu, Meijun ^{[2
]}

Wang, Xin ^{[1
,2
]}

Han, Lingling ^{[1
,2
]}

Luo, Shuang ^{[2
]}

机构：

[1] Chengdu Univ Tradit Chinese Med, Sch Med & Life Sci, Chengdu, Peoples R China

[2] Suining Cent Hosp, Dept Gynecol, Suining 629000, Peoples R China

来源：

CANCER REPORTS | 2024年 / 7卷 / 05期

关键词：

acute abdomen; chemotherapy; extrarenal malignant rhabdoid tumor; greater omentum; ADENOCARCINOMA; FEATURES; ILEUM; LUNG;

D O I：

10.1002/cnr2.2086

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

BackgroundMalignant extrarenal rhabdoid tumor (MERT) is a rare and highly metastatic tumor, which is more than 75% of patients dying within 6 months of initial diagnosis, and it often leads to misdiagnosis and delayed treatment.CaseThis paper reports a 16-year-old girl who presented with the chief complaint of acute abdominal pain. She underwent laparoscopic exploration and excisional biopsy, then pathological examination and immunohistochemistry revealed "extrarenal malignant rhabdomyoma." One month after operation, she died of intra-abdominal hemorrhage and multiple organ dysfunction.ConclusionMERT were often misdiagnosed and had a poor prognosis. The surgery and chemotherapy are usually beneficial to prolong the survival time of patients with MERT.

引用

页数：7

共 31 条

[1] Poorly differentiated adenocarcinoma with extensive rhabdoid differentiation: Clinicopathological features of two cases arising in the gastrointestinal tract [J].

Al-Nafussi, A ;

O'Donnell, M .

PATHOLOGY INTERNATIONAL, 1999, 49 (02) :160-163

[2]

Amrikachi Mojghan, 2002, Ann Diagn Pathol, V6, P357, DOI 10.1053/adpa.2002.36657

[3] Good Response to Chemotherapy Spares Irradiation for Extrarenal Rhabdoid Tumor Conferring Better Activities of Daily Living [J].

Asada, Nariaki ;

Kato, Itaru ;

Daifu, Tomoo ;

Umeda, Katsutsugu ;

Hiramatsu, Hidefumi ;

Okamoto, Takeshi ;

Toguchida, Junya ;

Yamawaki, Satoko ;

Yoshikawa, Katsuhiro ;

Adachi, Souichi ;

Heike, Toshio ;

Watanabe, Kenichiro .

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2015, 37 (01) :E57-E59

[4]

BECKWITH JB, 1978, CANCER-AM CANCER SOC, V41, P1937, DOI 10.1002/1097-0142(197805)41:5<1937::AID-CNCR2820410538>3.0.CO

[5]

2-U

[6] Frequent hSNF5/INI1 Germline Mutations in Patients with Rhabdoid Tumor [J].

Bourdeaut, Franck ;

Lequin, Delphine ;

Brugieres, Laurence ;

Reynaud, Stephanie ;

Dufour, Christelle ;

Doz, Francois ;

Andre, Nicolas ;

Stephan, Jean-Louis ;

Perel, Yves ;

Oberlin, Odile ;

Orbach, Daniel ;

Bergeron, Christophe ;

Rialland, Xavier ;

Freneaux, Paul ;

Ranchere, Dominique ;

Figarella-Branger, Dominique ;

Audry, Georges ;

Puget, Stephanie ;

Evans, D. Gareth ;

Ferreres Pinas, Joan Carles ;

Capra, Valeria ;

Mosseri, Veronique ;

Coupier, Isabelle ;

Gauthier-Villars, Marion ;

Pierron, Gaelle ;

Delattre, Olivier .

CLINICAL CANCER RESEARCH, 2011, 17 (01) :31-38

[7]

Cavazza A, 1996, AM J CLIN PATHOL, V105, P182

[8] Poorly differentiated cecal adenocarcinoma showing prominent rhabdoid feature combined with appendiceal mucinous cystadenoma: A case report and review of the literature [J].

Cho, In-Ju ;

Kim, Sung-Soo ;

Min, Young-Don ;

Noh, Mun-Whan ;

Hong, Ran .

ONCOLOGY LETTERS, 2015, 9 (04) :1527-1530

[9] Extraordinary disease-free survival in a rare malignant extrarenal rhabdoid tumor: A case report and review of the literature [J].

D'Amico F. ;

Bertacco A. ;

Cesari M. ;

Mescoli C. ;

Caturegli G. ;

Gondolesi G. ;

Cillo U. .

Journal of Medical Case Reports, 12 (1)

[10]

Fanburg-Smith J C, 1998, Ann Diagn Pathol, V2, P351, DOI 10.1016/S1092-9134(98)80038-5

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