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首页> 外文期刊>Journal of Indian association of pediatric surgeons >Concurrent congenital fibrolipomatous hamartoma and congenital nevus of infancy: A syndromic or chance association
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Concurrent congenital fibrolipomatous hamartoma and congenital nevus of infancy: A syndromic or chance association

机译:并发先天性纤维脂瘤性错构瘤和婴儿先天性痣:综合征或偶然关联

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Congenital nevi and fibrolipomatous hamartoma are benign tumors of childhood, the latter being very uncommon. Fibrous hamartoma of infancy typically occurs in <2 years of life. The concurrence of these two lesions is extremely rare. We report a case of congenital fibrolipomatous hamartoma and congenital nevus of infancy in a 6-month-old male infant. Clinically, a suspicion of benign versus malignant lesion beneath the giant congenital nevus prompted its surgical removal. The histopathology confirmed it to be a compound lesion with benign melanocytic nevi and fascicles of spindle cells with eosinophilic cytoplasm representing hamartoma. Several types of melanocytic combined lesions have been noted with neuroectodermal and mesenchymal components. Sometimes, malignant soft-tissue neoplasm such as liposarcoma, rhabdomyosarcoma, and ganglioneuroblastoma do occur. This case report highlights the role of prompt surgical excision and histopathological examination.
机译:先天性痣和纤维脂瘤性错构瘤是儿童的良性肿瘤,后者很少见。婴儿纤维错构瘤通常发生在生命的2年以下。这两个病变的并发极为罕见。我们报告了一个6个月大的男婴先天性纤维脂瘤性错构瘤和先天性痣的病例。临床上,怀疑是先天性巨痣下方的良性和恶性病变促使其手术切除。组织病理学证实它是具有良性黑素细胞痣和纺锤状细胞的分束的复合病灶,其中嗜酸性细胞质代表错构瘤。已经注意到几种类型的黑素细胞合并病变,具有神经外胚层和间充质成分。有时会发生恶性软组织肿瘤,例如脂肪肉瘤,横纹肌肉瘤和神经节神经母细胞瘤。该病例报告突出了及时手术切除和组织病理学检查的作用。

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