Enam Syed Faaiz, Waqas Muhammad, Rauf Muhammad Yaseen, Bari Muhammad Ehsan
Department of Biological and Biomedical Sciences, Aga Khan University, Karachi, Sindh, Pakistan.
BMJ Case Rep. 2014 Apr 23;2014:bcr2013202588. doi: 10.1136/bcr-2013-202588.
We present a case of congenital malignant melanoma of the scalp in a neonate. The child was born through caesarean section with a swelling, the size of a tennis ball, on the posterior scalp. At presentation to the clinic at 25 days after birth, the swelling had significantly increased in size and ulcerated. An excision was carried out but, because of extensive haemorrhage and haemodynamic instability, the procedure was limited to subtotal resection. Later on, completion of the excision and flap coverage of the wound were performed. After an initial stable course of a few months, the child came back with local recurrence. A re-excision was planned but the child developed pneumonia resulting in sepsis leading to the demise of the child. The report adds to the literature by describing a rare entity and challenges of managing large vascular scalp lesions with complete excision and defect coverage.
我们报告一例新生儿头皮先天性恶性黑色素瘤病例。该患儿通过剖宫产出生,后头皮有一个网球大小的肿物。出生25天后到诊所就诊时,肿物大小显著增大且发生了溃疡。进行了切除手术,但由于广泛出血和血流动力学不稳定,手术仅限于次全切除。后来,完成了切除并对伤口进行了皮瓣覆盖。在最初几个月病情稳定后,患儿出现局部复发。计划再次切除,但患儿患上肺炎导致败血症,最终死亡。该报告通过描述一种罕见病例以及完整切除和覆盖头皮大血管病变的管理挑战,丰富了文献资料。