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一例真性鼻上颌部婴儿纤维肉瘤的初步报告：单模式治疗及两年随访

Preliminary Report of a True NasoMaxillary Infantile Fibrosarcoma: Single-Modality Management and 2-Year Follow-Up.

作者信息

Jayakumar Naveenkumar, Rathnaprabhu Veerabahu, Ramesh Singaravelu

机构信息

Department of Oral and Maxillofacial Surgery, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.

Department of Paediatric Dentistry, Kanchi Kamakoti Childs Trust Hospital, Chennai, Tamil Nadu, India.

出版信息

Ann Maxillofac Surg. 2019 Jan-Jun;9(1):208-210. doi: 10.4103/ams.ams_281_18.

DOI:10.4103/ams.ams_281_18
PMID:31293956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6585220/
Abstract

Infantile fibrosarcoma (IFS) is a malignant tumor, commonly presenting in long bones and seldom encountered after 2 years of age. It is extremely rare in the faciomaxillary region. The condition is often mistaken for teratomas, and histopathology/immunohistochemistry is confirmatory. Treatment involves surgical resection as primary modality. Prognosis is much better compared to the adult variant with even scope for spontaneous regression following "conservative" resection. We present a case of IFS of the nasomaxillary complex in a 3-month-old female child. We managed our case with surgical resection, and the patient has remained disease free for over 2 years.

摘要

婴儿纤维肉瘤（IFS）是一种恶性肿瘤，常见于长骨，2岁以后很少见。在面颌部极为罕见。这种情况常被误诊为畸胎瘤，组织病理学/免疫组织化学检查可确诊。治疗以手术切除为主要方式。与成人型相比，其预后要好得多，甚至在“保守”切除后有自发消退的可能。我们报告一例3个月大女童鼻上颌复合体的婴儿纤维肉瘤病例。我们通过手术切除治疗该病例，患者已无病生存超过2年。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/22f87302e7c1/AMS-9-208-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/9e3098228c3d/AMS-9-208-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/89f675816b74/AMS-9-208-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/9481ce03c9be/AMS-9-208-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/382094674323/AMS-9-208-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/22f87302e7c1/AMS-9-208-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/9e3098228c3d/AMS-9-208-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/89f675816b74/AMS-9-208-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/9481ce03c9be/AMS-9-208-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/382094674323/AMS-9-208-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f297/6585220/22f87302e7c1/AMS-9-208-g005.jpg

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本文引用的文献

1
Infantile Fibrosarcoma of Tongue: A Rare Tumor.婴儿舌部纤维肉瘤：一种罕见肿瘤。
APSP J Case Rep. 2016 Jun 15;7(3):23. doi: 10.21699/ajcr.v7i3.432. eCollection 2016 Jul-Aug.
2
Primary fibrosarcoma of maxilla in an 8-year-old child: A rare entity.一名8岁儿童上颌骨原发性纤维肉瘤：一种罕见病例。
J Oral Maxillofac Pathol. 2013 Sep;17(3):478. doi: 10.4103/0973-029X.125226.
3
Infantile fibrosarcoma: clinical and histologic responses to cytotoxic chemotherapy.婴儿纤维肉瘤：细胞毒性化疗的临床及组织学反应
Pediatr Blood Cancer. 2009 Jul;53(1):23-7. doi: 10.1002/pbc.21981.
4
Fibrosarcoma of the head and neck. The UCLA experience.头颈部纤维肉瘤。加州大学洛杉矶分校的经验。
Arch Otolaryngol Head Neck Surg. 1991 Apr;117(4):396-401. doi: 10.1001/archotol.1991.01870160050007.