Sokol Jason A, Clark Jeremy D, Lee Hui Bae Harold, Nunery William R
Department of Ophthalmology and Visual Sciences, University of Louisville, Louisville, Kentucky, USA.
J Pediatr Ophthalmol Strabismus. 2010 Oct 21;47 Online:e1-4. doi: 10.3928/01913913-20101018-07.
An 8-year-old girl with a history of microphthalmia in the right eye presented with a left medial upper eyelid mass with a dark blue-green nodule that could be seen through the skin but did not appear to involve the overlying epidermis. A biopsy demonstrated a pigmented epithelioid melanocytoid tumor with rare mitoses arising in association with a congenital nevus and positive margins. Due to the pathological findings, the patient underwent excision of the tumor with 5-mm margins and a sentinel lymph node biopsy. The re-excision of the upper eyelid margins demonstrated residual benign congenital melanocytic nevus, but did not reveal residual melanocytic lesion. The parotid sentinel node biopsy revealed benign and cytologically mature nevus nests in the capsule and septa, but there was no evidence of involvement with the pigmented epithelioid melanocytoid tumor. The patient underwent successful eyelid reconstruction and had no evidence of recurrence or metastasis after 2 years.
一名8岁女童,右眼有小眼症病史,其左上眼睑出现肿物,肿物上有一个蓝绿色小结节,透过皮肤可见,但似乎未累及上方表皮。活检显示为色素性上皮样黑素细胞肿瘤,有罕见的核分裂象,与先天性痣相关,切缘阳性。鉴于病理检查结果,患者接受了肿瘤切除,切缘为5毫米,并进行了前哨淋巴结活检。对上眼睑切缘再次切除显示残留良性先天性黑素细胞痣,但未发现残留黑素细胞病变。腮腺前哨淋巴结活检显示,包膜和间隔中有良性且细胞学成熟的痣巢,但没有证据表明色素性上皮样黑素细胞肿瘤累及。患者眼睑重建成功,2年后无复发或转移迹象。