A Persistent Dark Macule on the Hand of a Hispanic Patient.

Fanny Cecilia Cordero-Martinez, Adrian Cuellar-Barboza, Jorge Ocampo-Candiani
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Abstract

A 38-year-old Hispanic man without comorbidities presented to our dermatology clinic for the evaluation of an asymptomatic dark macule on his left hand, which had gradually grown since he was a child. The hyperpigmentation involved the dorsum and palm (Figure 1). The patient was right-handed and denied previous trauma, inflammation, occupational exposure to chemicals, or using any medications. During physical examination, no other similar pigmentation was found on the rest of his body. An incisional biopsy of the left palm was performed (Figure 2). The histopathology revealed the presence of spindle-shaped cells with melanin granules in the superficial and middle dermis, surrounding the blood vessels, and between collagen bundles, which are findings compatible with acquired dermal melanocytosis (1,2). On dermoscopy, we found a pattern of regular pigment with a gray-brown tone and whitish spots within. We discussed the benignity of this rare entity with the patient, and he decided not to pursue treatment. Acquired dermal melanocytosis (ADM) is a rare condition, with isolated presentation on the hand and with less than 10 cases reported (1). Dermal melanocytosis includes several benign pigmented lesions histologically characterized by the presence of melanocytes in the dermis, which are spindle-shaped dendritic cells containing brown melanin pigment. Melanocytes can also be identified with immunoperoxidase staining for S100 and Fontana-Masson melanin stain (2). The physiopathology of ADM remains unclear, but it has been proposed that it involves reactivation of latent dermal melanocytes due to external factors such as trauma, inflammation, chemical exposure, sunlight, drugs, and hormonal treatment with estrogen and/or progesterone (3). ADM with hand involvement usually appears in the Asian population without sex predilection. The lesions develop in adolescence or young adulthood and tend to affect both hands and other body areas such as the face or the legs; there have also been two reported cases in the Hispanic population (both by Fitzpatrick III) (3,4). ADM must be differentiated from ectopic Mongolian spots, plaque-type blue nevi, tinea nigra, or other pigmented neoplasms. A biopsy is mandatory to establish a proper diagnosis. Ectopic Mongolian spots and plaque-type blue nevi are both congenital dermal melanocytoses that may present as bluish macules on the hand. However, these lesions show deep and more widely scattered distribution of melanocytes (1). There have also been some reports of malignant melanoma and acquired dermal melanocytosis that appeared on congenital nevus spilus (5). ADM is a benign condition, and reassurance should be offered to these patients.

一位西班牙裔患者手部的顽固黑斑。
一名无合并症的 38 岁西班牙裔男子到我院皮肤科就诊,他的左手上有一个无症状的深色斑丘疹,自孩提时代起就逐渐增大。色素沉着涉及手背和手掌(图 1)。患者是右撇子,否认曾有外伤、炎症、职业性接触化学物质或使用任何药物。体格检查时,在他身体的其他部位没有发现类似的色素沉着。医生对患者的左手掌进行了切口活检(图 2)。组织病理学检查发现,在真皮浅层和中层、血管周围以及胶原束之间存在带有黑色素颗粒的纺锤形细胞,这些结果与获得性真皮黑色素细胞增多症相符(1,2)。在皮肤镜检查中,我们发现了一种灰褐色调的规则色素斑,内部有白色斑点。我们与患者讨论了这种罕见病的良恶性,他决定不再继续治疗。获得性真皮黑素细胞增多症(ADM)是一种罕见病,仅在手部出现,目前报道的病例不到 10 例(1)。真皮黑素细胞增多症包括几种良性色素病变,组织学特征是真皮中存在黑素细胞,它们是纺锤形树突状细胞,含有棕色黑素。黑色素细胞也可通过 S100 免疫过氧化物酶染色法和 Fontana-Masson 黑色素染色法鉴别出来(2)。ADM 的生理病理尚不清楚,但有人认为它涉及潜伏的真皮黑色素细胞因创伤、炎症、化学暴露、日光、药物和使用雌激素和/或孕酮的激素治疗等外部因素而重新激活(3)。手部受累的 ADM 通常出现在亚洲人群中,无性别偏好。病变发生在青春期或青年期,往往累及双手和其他身体部位,如面部或腿部;在西班牙裔人群中也有两例报道(均为菲茨帕特里克三世病例)(3,4)。ADM 必须与异位蒙古斑、斑块型蓝痣、黑色素痣或其他色素性肿瘤相鉴别。要确定正确的诊断,必须进行活检。异位蒙古斑和斑块型蓝痣都是先天性真皮黑素细胞增多症,可能表现为手部淡蓝色斑丘疹。不过,这些病变的黑素细胞分布较深且较分散(1)。也有一些关于恶性黑色素瘤和后天性真皮黑素细胞增多症的报道,它们出现在先天性黑痣上(5)。ADM 是一种良性病变,应向这些患者提供安慰。
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