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[炎性幼年性结膜痣(IJCN)]

[Inflammatory juvenile conjunctival nevus (IJCN)].

作者信息

Lommatzsch P K, Willerding G, Nenning H, Taubert G

机构信息

Augenärztliche Gemeinschaftspraxis, Leipzig.

出版信息

Klin Monbl Augenheilkd. 2007 May;224(5):422-6. doi: 10.1055/s-2007-963065.

Abstract

BACKGROUND

Pathologists may occasionally have difficulties in reliably assessing the dignity of tumour cells in histological sections, especially in nevi with junctional activity.

PATIENT HISTORY

This case history of a boy suffering from an inflammatory juvenile conjunctival nevus (IJCN) is reported with a follow-up period of 25 years. Seven years after first surgical treatment of a histologically proven nevus, a recurrent pigmented lesion within the former operation area aroused the suspicion of it being a malignant melanoma. Logically, a second excision was performed followed by cryotherapy with liquid nitrogen (spray freezing). The histological diagnosis performed by a pathologist resulted in a malignant melanoma. A second recurrent pigmented conjunctival tumour developed fourteen years later. This lesion again aroused another strong clinical suspicion of malignant transformation into a melanoma. However, the histological examination of the biopsy at this time only showed benign nevus cells and areas of conjunctival melanosis without atypia.

DISCUSSION

Especially in young patients, IJCN must be regarded as an independent type of nevus, which might lead even experts in ophthalmic pathology to over-diagnose this lesion as a malignant melanoma. This could mean that the wrong therapeutic steps were taken with surgical procedures that cause unnecessary mutilation. A reappraisal of the former histological specimens of the first recurrent tumour by other pathologists came to the conclusion that the initial diagnosis of melanoma could not be maintained. Nevertheless, we also strongly recommend follow-up examinations at regular intervals in cases of IJCN since we are aware of the fact that melanocytic tumours of the conjunctiva behave unpredictably.

摘要

背景

病理学家在通过组织学切片可靠评估肿瘤细胞的特性时偶尔会遇到困难,尤其是在具有交界活性的痣中。

患者病史

本文报告了一名患有炎症性幼年结膜痣(IJCN)男孩的病例,随访期为25年。在对组织学确诊的痣进行首次手术治疗7年后,原手术区域内复发性色素沉着病变引发了恶性黑色素瘤的怀疑。顺理成章地,进行了第二次切除,随后用液氮进行冷冻治疗(喷雾冷冻)。病理学家进行的组织学诊断结果为恶性黑色素瘤。14年后出现了第二个复发性色素沉着性结膜肿瘤。该病变再次引发了强烈的临床怀疑,即已恶变成为黑色素瘤。然而,此时活检的组织学检查仅显示良性痣细胞和无异型性的结膜黑变病区域。

讨论

尤其是在年轻患者中,IJCN必须被视为一种独立类型的痣,这可能导致即使是眼科病理学专家也会将该病变过度诊断为恶性黑色素瘤。这可能意味着采取了错误的治疗步骤,进行了导致不必要损伤的外科手术。其他病理学家对第一个复发性肿瘤的先前组织学标本进行重新评估后得出结论,最初的黑色素瘤诊断不能成立。尽管如此,我们也强烈建议对IJCN病例进行定期随访检查,因为我们知道结膜黑素细胞肿瘤的行为不可预测。

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