Dey Soumya, Mandal Bappa, Chatterjee Uttara, Mukherjee Suchandra
Department of Pathology, Institute of Post Graduate Medical Education and Research, Kolkata, West Bengal, India.
Department of Neonatology, Institute of Post Graduate Medical Education and Research, Kolkata, West Bengal, India.
J Indian Assoc Pediatr Surg. 2022 Nov-Dec;27(6):756-759. doi: 10.4103/jiaps.jiaps_14_22. Epub 2022 Nov 14.
Infantile myofibromas (IMs) are benign soft-tissue tumors of children. They are of fibroblastic-myofibroblastic origin and show considerable morphological overlap with other spindle cell neoplasms. Here, we present two cases of solitary myofibromas, one in a neonate and one in a 2-year-old girl. A 2-day-old girl presented with severe respiratory distress and died during intubation. At autopsy, a myofibroma involving the oropharynx with extension up to the larynx was noted. Second case was a 2-year-girl with a myofibroma in the hard palate. IM must be differentiated from other benign and malignant spindle cell tumors of infancy and childhood. Oropharyngeal myofibroma should be considered in the differentials of neonatal respiratory distress.
婴儿肌纤维瘤(IMs)是儿童的良性软组织肿瘤。它们起源于成纤维细胞-肌成纤维细胞,与其他梭形细胞肿瘤在形态学上有相当大的重叠。在此,我们报告两例孤立性肌纤维瘤病例,一例发生在新生儿,另一例发生在一名2岁女孩。一名2日龄女婴出现严重呼吸窘迫,在插管过程中死亡。尸检时,发现一个肌纤维瘤累及口咽并延伸至喉部。第二例是一名2岁女孩,硬腭有一个肌纤维瘤。IM必须与婴儿期和儿童期的其他良性和恶性梭形细胞肿瘤相鉴别。口咽肌纤维瘤应列入新生儿呼吸窘迫的鉴别诊断中。