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Treatment of Abdominal Desmoplastic Small Round Cell Tumor Induces Acute Myeloid Leukemia-M5: A Case Report and Literature Review.
Liu, Lan; Zhong, Meizuo; Zhou, Xuan; Kang, Fanhua; Long, Yong; Li, Junfeng.
Afiliação
  • Liu L; Department of Oncology, Xiangya Changde Hospital, Changde, Hunan, People's Republic of China.
  • Zhong M; Department of Oncology, Xiangya Changde Hospital, Changde, Hunan, People's Republic of China.
  • Zhou X; Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
  • Kang F; Department of Hematology, Xiangya Changde hospital, Changde, Hunan, People's Republic of China.
  • Long Y; Department of Pathology, Xiangya Changde Hospital, Changde, Hunan, People's Republic of China.
  • Li J; Department of Oncology, Xiangya Changde Hospital, Changde, Hunan, People's Republic of China.
Onco Targets Ther ; 17: 163-169, 2024.
Article em En | MEDLINE | ID: mdl-38435840
ABSTRACT
Desmoplastic small round cell tumor (DSRCT) is a rare and highly aggressive malignancy. Most patients are diagnosed at a late stage with poor prognosis. The treatment usually includes combined intensive chemotherapy, cytoreductive surgery, radiotherapy, and targeted therapy. Due to the low incidence rate and dismal survival, there is currently a lack of case reports on DSRCT with concurrent leukemia. We report a case of a young patient who achieved disease stabilization for 14 months after receiving 6 cycles of chemotherapy and whole abdominal radiation therapy (WART), followed by consolidation treatment with anlotinib. However, the treatment was terminated due to the development of Acute Myeloid Leukemia-M5 (AML-M5). Multimodal therapy may provide a survival benefit for rare tumors that lack standard treatment. However, intensive chemotherapy and extensive radiotherapy carry a risk of inducing secondary malignancies. This is the first reported case of concurrent DSRCT and AML-M5 with short intervals between onset.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article