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乳头原发性黑色素瘤:10例报告,包括与佩吉特病并存的情况。

Primary melanoma of the nipple: Report of 10 cases including coexistence with Paget's disease.

作者信息

Dehner Carina A, Johnson Emma F, Peters Margot S, Guo Ruifeng Ray

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA; Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.

Department of Dermatology, Mayo Clinic, Rochester, MN 55905, USA; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Pathol Res Pract. 2024 Jan;253:155058. doi: 10.1016/j.prp.2023.155058. Epub 2023 Dec 22.

Abstract

Primary melanoma of the nipple (PMN) is exceedingly rare, with only single cases reported to date. We identified 10 patients with PMN: 5 females, 5 males, median age 55.5 years (range 29-66) at diagnosis of melanoma in situ (4 cases) or invasive melanoma (6 cases, Breslow depth 0.2 mm to 3.5 mm). Follow-up was available for all 10 patients (median 19 months, range 1-183). Nine patients had no evidence of disease; one patient died of disease (13.5 months) after presenting with a nodal metastasis. One case was exceptional, because the patient presented with a pigmented lesion that histopathologically exhibited co-existence of melanoma in situ and Paget disease, a challenging differential diagnosis due to immunohistochemical pitfalls in distinction between melanoma in situ and the pigmented variant of mammary Paget disease. Here we report the second largest series of PMN including a case of PMN colliding with mammary Paget disease, to raise awareness of these rare malignancies.

摘要

乳头原发性黑色素瘤(PMN)极为罕见,迄今为止仅有个别病例报道。我们确定了10例PMN患者:5名女性,5名男性,诊断为原位黑色素瘤(4例)或浸润性黑色素瘤(6例,Breslow深度0.2毫米至3.5毫米)时的中位年龄为55.5岁(范围29 - 66岁)。所有10例患者均有随访资料(中位随访时间19个月,范围1 - 183个月)。9例患者无疾病证据;1例患者出现淋巴结转移后死于疾病(13.5个月)。有1例情况特殊,该患者出现一个色素沉着病变,组织病理学显示原位黑色素瘤与佩吉特病并存,由于原位黑色素瘤与乳腺佩吉特病色素沉着变体在免疫组化鉴别上存在陷阱,这是一个具有挑战性的鉴别诊断。在此,我们报告第二大系列的PMN病例,包括1例PMN与乳腺佩吉特病并存的病例,以提高对这些罕见恶性肿瘤的认识。

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