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婴儿期原始黏液样间叶肿瘤：一场失败的战斗。

Primitive Myxoid Mesenchymal Tumor of Infancy: A Lost Battle.

作者信息

Peters Nitin James, Reddy V Manasa, Bal Amanjit, Jain Arihant, Gupta Anjali, Madan Renu, Mahajan Jai Kumar

机构信息

Department of Pediatric Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Department of Histopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

J Indian Assoc Pediatr Surg. 2024 Nov-Dec;29(6):637-639. doi: 10.4103/jiaps.jiaps_103_24. Epub 2024 Nov 5.

DOI:10.4103/jiaps.jiaps_103_24
PMID:39691925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11649055/
Abstract

Primitive myxoid mesenchymal tumor of infancy (PMMTI) is a low to intermediate-grade, poorly differentiated myofibroblastic tumor and is characterized by its tendency to recur locally. It commonly occurs in the 1 year of life and is predominantly seen in the axial skeleton and rarely in the retroperitoneum. We report one such case of PMMTI, which is the second case reported in English literature.

摘要

婴儿原始黏液样间叶性肿瘤（PMMTI）是一种低至中级别的、低分化肌成纤维细胞肿瘤，其特点是有局部复发倾向。它通常发生在1岁以内，主要见于中轴骨骼，很少见于腹膜后。我们报告了一例这样的PMMTI病例，这是英文文献中报道的第二例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d5/11649055/b1fe62bf2d23/JIAPS-29-637-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d5/11649055/fe1b5308d828/JIAPS-29-637-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d5/11649055/d5a1b97b7fc5/JIAPS-29-637-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d5/11649055/b1fe62bf2d23/JIAPS-29-637-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d5/11649055/fe1b5308d828/JIAPS-29-637-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d5/11649055/d5a1b97b7fc5/JIAPS-29-637-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d5/11649055/b1fe62bf2d23/JIAPS-29-637-g003.jpg

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本文引用的文献

1
Primitive myxoid mesenchymal tumor of infancy with brain metastasis: first reported case.婴儿期原发性黏液样间充质肿瘤伴脑转移：首例报告病例
Childs Nerv Syst. 2019 Feb;35(2):363-368. doi: 10.1007/s00381-018-3964-x. Epub 2018 Sep 3.
2
Recurrent BCOR Internal Tandem Duplication and YWHAE-NUTM2B Fusions in Soft Tissue Undifferentiated Round Cell Sarcoma of Infancy: Overlapping Genetic Features With Clear Cell Sarcoma of Kidney.婴儿软组织未分化圆形细胞肉瘤中的复发性BCOR内部串联重复和YWHAE-NUTM2B融合：与肾透明细胞肉瘤重叠的遗传特征
Am J Surg Pathol. 2016 Aug;40(8):1009-20. doi: 10.1097/PAS.0000000000000629.
3
A cooperative approach to diagnosis of rare diseases: primitive myxoid mesenchymal tumor of infancy.
罕见病诊断的协作方法：婴儿期原始黏液样间叶肿瘤
Ann Clin Lab Sci. 2014 Summer;44(3):310-6.
4
Primitive myxoid mesenchymal tumor of infancy: a report of a further case with locally aggressive behavior.婴儿期原始黏液样间叶性肿瘤：1例具有局部侵袭性行为的病例报告
Pediatr Dev Pathol. 2011 Jan-Feb;14(1):75-9. doi: 10.2350/09-12-0770-CR.1. Epub 2010 May 13.
5
Primitive myxoid mesenchymal tumor of infancy: a clinicopathologic report of 6 cases.婴儿原始黏液样间叶肿瘤：6例临床病理报告
Am J Surg Pathol. 2006 Mar;30(3):388-94. doi: 10.1097/01.pas.0000190784.18198.d8.