Esmaeili Heidarali, Azimpouran Mahzad
Department of General pathology, Tabriz University of Medical Science, Tabriz, Iran.
Int J Surg Case Rep. 2017;31:47-50. doi: 10.1016/j.ijscr.2016.12.013. Epub 2017 Jan 5.
Congenital or neonatal rhabdomyosarcoma (RMS) is a rare soft tissue tumor with the most common sites of origin in genitourinary tract, head, and neck regions and extremities are less commonly involved.
In this paper, a case of embryonal RMS with skin lesions, lymph nodes metastasis, and bone marrow metastasis is reported for a 1-month old female patient.
This study presents how within 8-months of chemotherapy, the lesions got subsided and the patient became disease free.
Multiple congenital rhabdomyosarcoma of neonate is a rare finding that should be considered as differential diagnosis of lymphoma and neurofibroma.
先天性或新生儿横纹肌肉瘤（RMS）是一种罕见的软组织肿瘤，最常见的起源部位是泌尿生殖道、头颈部，四肢较少受累。
本文报告了一名1个月大的女性患者，患有伴有皮肤病变、淋巴结转移和骨髓转移的胚胎性RMS。
本研究展示了在化疗8个月内，病变如何消退且患者实现无病状态。
新生儿多发性先天性横纹肌肉瘤是一种罕见的发现，应作为淋巴瘤和神经纤维瘤的鉴别诊断考虑。
