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孕期原发性骨组织细胞肉瘤患者的风险权衡:病例报告及文献综述

Balancing risk in a patient with primary bone histiocytic sarcoma during pregnancy: Case report and review of the literature.

作者信息

Al-Amri Ayman, Al-Khabori Murtadha, Al-Riyami Nihal, Al-Haddabi Ibrahim

机构信息

Surgery Department, Sultan Qaboos University Hospital, Muscat, Oman.

Haematology Department, Sultan Qaboos University Hospital, Muscat, Oman.

出版信息

Int J Surg Case Rep. 2021 Jun;83:106021. doi: 10.1016/j.ijscr.2021.106021. Epub 2021 May 26.

Abstract

INTRODUCTION AND IMPORTANCE

Histiocytic sarcoma (HS) is a rare, aggressive malignant neoplasm of hematopoietic cell origin. Primary HS of the proximal humerus, without involvement of lymph nodes or bone marrow, or systemic features, is very rare.

CASE PRESENTATION

We report a rare case of primary bony HS of the proximal humerus without bone marrow involvement in a healthy 33-year-old pregnant woman. She was successfully treated with surgical resection during pregnancy and radiotherapy post-delivery.

CLINICAL DISCUSSION

This is the first report of a patient with primary bony HS during pregnancy. This highlights the fact that although HS is a neoplasm of hemolymphoid cell lineage, it frequently arises in non-lymphoid organs.

CONCLUSION

This case emphasizes the importance of a multidisciplinary approach and the need for balancing treatment risk in a patient with primary bone HS during pregnancy.

摘要

引言与重要性

组织细胞肉瘤(HS)是一种罕见的、侵袭性的造血细胞源性恶性肿瘤。肱骨近端的原发性HS,无淋巴结或骨髓受累,亦无全身症状,极为罕见。

病例介绍

我们报告一例罕见的肱骨近端原发性骨HS病例,患者为一名33岁的健康孕妇,无骨髓受累。她在孕期接受了手术切除,并在产后接受了放疗,治疗成功。

临床讨论

这是首例关于孕期原发性骨HS患者的报告。这凸显了一个事实,即尽管HS是一种血液淋巴细胞谱系的肿瘤,但它经常发生于非淋巴器官。

结论

本病例强调了多学科方法的重要性,以及在孕期原发性骨HS患者中平衡治疗风险的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f95/8178090/ac24924cf8e1/gr1.jpg

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