Iwafuchi Hideto, Tsuzuki Toyonori, Ito Rieko, Miyake Hiromu, Okita Hajime, Hamazaki Minoru
Department of Pathology, National Center for Child Health and Development, Tokyo, Japan.
Department of Pathology, Shizuoka Children's Hospital, Shizuoka, Japan.
Pathol Int. 2015 Aug;65(8):432-7. doi: 10.1111/pin.12312. Epub 2015 May 20.
Infantile myofibromatosis (IM) is a rare disorder present at birth or in early infancy with a biphasic histological pattern. We present a neonatal-onset case of generalized IM with visceral (central nervous system, heart, lungs, liver, spleen, small intestine, kidneys and bones) and placental involvement, showing a monophasic histological pattern through the lesions during the course of disease. Histologically, the tumor was composed of a solid proliferation of cytologically uniform, 'primitive' mesenchymal cells associated with a hemangiopericytoma-like vascular pattern. Immunohistochemical analysis and ultrastructural study revealed that the tumor cells exhibited primitive features without mature myofibroblastic differentiation. Neither ETV6-NTRK3 nor ACTB-GLI fusion gene was identified. The patient died of cerebral hemorrhage and respiratory failure at four months of age despite intensive therapy. Generalized IM characterized by monophasic primitive pattern could be related to poor clinical outcome.
婴儿肌纤维瘤病(IM)是一种在出生时或婴儿早期出现的罕见疾病,具有双相组织学模式。我们报告一例新生儿期发病的全身性IM病例,伴有内脏(中枢神经系统、心脏、肺、肝脏、脾脏、小肠、肾脏和骨骼)及胎盘受累,在疾病过程中病变呈现单相组织学模式。组织学上,肿瘤由细胞学上一致的“原始”间充质细胞实性增生构成,伴有类似血管外皮细胞瘤的血管模式。免疫组织化学分析和超微结构研究显示肿瘤细胞呈现原始特征,无成熟肌成纤维细胞分化。未检测到ETV6-NTRK3和ACTB-GLI融合基因。尽管进行了强化治疗,该患者在4个月大时死于脑出血和呼吸衰竭。以单相原始模式为特征的全身性IM可能与不良临床结局相关。