Peters Nitin James, Reddy V Manasa, Bal Amanjit, Jain Arihant, Gupta Anjali, Madan Renu, Mahajan Jai Kumar
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.
J Indian Assoc Pediatr Surg. 2024 Nov-Dec;29(6):637-639. doi: 10.4103/jiaps.jiaps_103_24. Epub 2024 Nov 5.
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.
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。
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