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肋骨小细胞骨肉瘤：一种罕见的发病部位。

Small cell osteosarcoma of the rib: An exceptional localization.

作者信息

Abid Walid, Triki Meriam, Hlima Ghassen Ben, Chaari Zied, Hentati Abdessalem, Frikha Imed

机构信息

University of Sfax Faculty of Medicine of Sfax, Cardiovascular and Thoracic Department Habib Bourguiba University Hospital Sfax Tunisia.

University of Sfax Faculty of Medicine of Sfax, Department of Pathology and Reasearch Laboratory LR18SP10 Habib Bourguiba University Hospital Sfax Tunisia.

出版信息

Clin Case Rep. 2022 Sep 23;10(9):e6377. doi: 10.1002/ccr3.6377. eCollection 2022 Sep.

DOI:10.1002/ccr3.6377
PMID:36188044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9500416/
Abstract

Small cell osteosarcoma is a rare sub-type of osteogenic malignant tumors. Rib localization is uncommon. Histological examination is an important step to make the difference with similar tumors like Ewing's sarcoma. Surgical resection is the unique curative treatment. The prognosis remains poor even with adjuvant treatment.

摘要

小细胞骨肉瘤是一种罕见的成骨性恶性肿瘤亚型。肋骨部位受累并不常见。组织学检查是与尤因肉瘤等相似肿瘤进行鉴别的重要步骤。手术切除是唯一的治愈性治疗方法。即使采用辅助治疗，预后仍然很差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/9ef7e74592e9/CCR3-10-e6377-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/bdd804730a87/CCR3-10-e6377-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/9758b87237dc/CCR3-10-e6377-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/5e69a1db02b0/CCR3-10-e6377-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/9ef7e74592e9/CCR3-10-e6377-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/bdd804730a87/CCR3-10-e6377-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/9758b87237dc/CCR3-10-e6377-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/5e69a1db02b0/CCR3-10-e6377-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e4/9500416/9ef7e74592e9/CCR3-10-e6377-g003.jpg

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本文引用的文献

1
Primary peripheral neuroectodermal tumor (PNET) of the adrenal gland: a rare entity.肾上腺原发性外周神经外胚层肿瘤（PNET）：一种罕见的实体瘤。
J BUON. 2019 Mar-Apr;24(2):770-778.
2
Small cell osteosarcoma of rib: diagnosis and treatment of the rare case.肋骨小细胞骨肉瘤：罕见病例的诊断与治疗
Tuberk Toraks. 2012;60(2):172-5.
3
Small cell osteogenic sarcoma of the ribs: cytological, immunohistochemical, and ultrastructural study with literature review.
Ultrastruct Pathol. 1999 Mar-Apr;23(2):133-40. doi: 10.1080/019131299281770.
4
Osteosarcoma of the proximal fibula: report of 3 cases.腓骨近端骨肉瘤：3例报告
Acta Chir Belg. 1997 Oct;97(5):260-3.
5
Small cell osteosarcoma of bone: an immunohistochemical study with differential diagnostic considerations.骨小细胞骨肉瘤：一项伴有鉴别诊断考量的免疫组织化学研究
Hum Pathol. 1993 Nov;24(11):1211-25. doi: 10.1016/0046-8177(93)90218-6.
6
Small-cell osteosarcoma.小细胞骨肉瘤
Cancer. 1982 Sep 1;50(5):990-6. doi: 10.1002/1097-0142(19820901)50:5<990::aid-cncr2820500529>3.0.co;2-r.
7
The ultrastructure of small-cell osteosarcoma, with a review of the light microscopy and differential diagnosis.
Hum Pathol. 1991 Mar;22(3):267-75. doi: 10.1016/0046-8177(91)90161-h.
8
Survival, prognosis, and therapeutic response in osteogenic sarcoma. The Memorial Hospital experience.
Cancer. 1992 Feb 1;69(3):698-708. doi: 10.1002/1097-0142(19920201)69:3<698::aid-cncr2820690317>3.0.co;2-g.