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De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients

OBJECTIVE: To describe myeloid sarcoma (MS) that mimic gynecological tumors and provide guidelines for improving the diagnosis and treatment of patients. METHODS: This case series study retrospectively analyzed the clinicopathological characteristics and oncological outcomes of female patients who w...

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Autores principales: Gu, Yu, Zheng, Haoran, Mo, Shengwei, Guo, Tao, Chen, Lihua, Yang, Junjun, Xiang, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053749/
https://www.ncbi.nlm.nih.gov/pubmed/36978050
http://dx.doi.org/10.1186/s12905-023-02278-3
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author Gu, Yu
Zheng, Haoran
Mo, Shengwei
Guo, Tao
Chen, Lihua
Yang, Junjun
Xiang, Yang
author_facet Gu, Yu
Zheng, Haoran
Mo, Shengwei
Guo, Tao
Chen, Lihua
Yang, Junjun
Xiang, Yang
author_sort Gu, Yu
collection PubMed
description OBJECTIVE: To describe myeloid sarcoma (MS) that mimic gynecological tumors and provide guidelines for improving the diagnosis and treatment of patients. METHODS: This case series study retrospectively analyzed the clinicopathological characteristics and oncological outcomes of female patients who were histologically diagnosed with MS after initially presenting with reproductive-system tumors at the Peking Union Medical College Hospital between January 2000 and March 2022. RESULTS: There were eight cases in which MS mimicked cervical cancer, ovarian cancer, or hysteromyoma. Six patients had isolated MS, and the other two had acute myeloid leukemia (AML)-M2. The average age was 39.00 ± 14.26. They each sought advice from a gynecological oncologist at the initial visit, complaining of irregular bleeding (3/8), low abdominal pain (3/8), dysmenorrhea (1/8), or an accidentally found mass (1/8). CT/MRI exams revealed that the average tumor size reached 5.65 ± 2.35 cm, with 50% of the tumors being larger than 8 cm. The final diagnoses were confirmed by biopsy (2/8) or postoperative pathology (6/8); the most frequent positive immunohistochemical markers were Ki-67 (60–90%), MPO (100%), LCA (62.5%), CD43 (62.5%), CD117 (62.5%), CD99 (50%), vimentin (37.5%), and lysozyme (25%). MLL/AF9 gene fusions and CEBPA, JAK2, NRAS, and FLT3-TKD mutations were found in the patients. Six (75%) of the patients showed a complete response after upfront treatment using chemotherapy + surgery and experienced no recurrence during follow-up. The overall survival (OS) rate was 72.9%, and the 5-year OS rate was 72.9% (95%CI: 0.4056–1.000). The median OS was 26 months (range: 3–82). CONCLUSION: For patients with isolated MS, treatment by chemotherapy and surgery are radical procedure, and initial treatment using chemotherapy alone should be considered for MS with synchronous intramedullary AML. Poor response to chemotherapy, short interval to leukemia occurrence, and heavy tumor burden (> 10 cm) could indicate a poor prognosis for patients with MS.
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spelling pubmed-100537492023-03-30 De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients Gu, Yu Zheng, Haoran Mo, Shengwei Guo, Tao Chen, Lihua Yang, Junjun Xiang, Yang BMC Womens Health Research OBJECTIVE: To describe myeloid sarcoma (MS) that mimic gynecological tumors and provide guidelines for improving the diagnosis and treatment of patients. METHODS: This case series study retrospectively analyzed the clinicopathological characteristics and oncological outcomes of female patients who were histologically diagnosed with MS after initially presenting with reproductive-system tumors at the Peking Union Medical College Hospital between January 2000 and March 2022. RESULTS: There were eight cases in which MS mimicked cervical cancer, ovarian cancer, or hysteromyoma. Six patients had isolated MS, and the other two had acute myeloid leukemia (AML)-M2. The average age was 39.00 ± 14.26. They each sought advice from a gynecological oncologist at the initial visit, complaining of irregular bleeding (3/8), low abdominal pain (3/8), dysmenorrhea (1/8), or an accidentally found mass (1/8). CT/MRI exams revealed that the average tumor size reached 5.65 ± 2.35 cm, with 50% of the tumors being larger than 8 cm. The final diagnoses were confirmed by biopsy (2/8) or postoperative pathology (6/8); the most frequent positive immunohistochemical markers were Ki-67 (60–90%), MPO (100%), LCA (62.5%), CD43 (62.5%), CD117 (62.5%), CD99 (50%), vimentin (37.5%), and lysozyme (25%). MLL/AF9 gene fusions and CEBPA, JAK2, NRAS, and FLT3-TKD mutations were found in the patients. Six (75%) of the patients showed a complete response after upfront treatment using chemotherapy + surgery and experienced no recurrence during follow-up. The overall survival (OS) rate was 72.9%, and the 5-year OS rate was 72.9% (95%CI: 0.4056–1.000). The median OS was 26 months (range: 3–82). CONCLUSION: For patients with isolated MS, treatment by chemotherapy and surgery are radical procedure, and initial treatment using chemotherapy alone should be considered for MS with synchronous intramedullary AML. Poor response to chemotherapy, short interval to leukemia occurrence, and heavy tumor burden (> 10 cm) could indicate a poor prognosis for patients with MS. BioMed Central 2023-03-29 /pmc/articles/PMC10053749/ /pubmed/36978050 http://dx.doi.org/10.1186/s12905-023-02278-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Gu, Yu
Zheng, Haoran
Mo, Shengwei
Guo, Tao
Chen, Lihua
Yang, Junjun
Xiang, Yang
De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients
title De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients
title_full De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients
title_fullStr De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients
title_full_unstemmed De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients
title_short De novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients
title_sort de novo myeloid sarcoma mimicking gynecological tumors: a retrospective case series of eight patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053749/
https://www.ncbi.nlm.nih.gov/pubmed/36978050
http://dx.doi.org/10.1186/s12905-023-02278-3
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