International journal of surgery case reports · 2017
Congenital embryonal rhabdomyosarcoma; multiple lesions.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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История · было → стало
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Esmaeili Heidarali, Azimpouran Mahzad
Аннотация
INTRODUCTION: 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.
PRESENTATION OF CASE: 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.
DISCUSSION: This study presents how within 8-months of chemotherapy, the lesions got subsided and the patient became disease free.
CONCLUSION: Multiple congenital rhabdomyosarcoma of neonate is a rare finding that should be considered as differential diagnosis of lymphoma and neurofibroma.
PRESENTATION OF CASE: 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.
DISCUSSION: This study presents how within 8-months of chemotherapy, the lesions got subsided and the patient became disease free.
CONCLUSION: Multiple congenital rhabdomyosarcoma of neonate is a rare finding that should be considered as differential diagnosis of lymphoma and neurofibroma.