Matsumoto Chinatsu, Niiyama Shiro, Nagata Takuya, Oharaseki Toshiaki, Fukuda Hidetsugu
Shiro Niiyama, MD, PhD Department of Dermatology, Toho University Ohashi Medical Center Ohashi, Meguro-ku, Tokyo, Japan
Acta Dermatovenerol Croat. 2022 Dec;30(4):263-264.
Dear Editor,Mammary Paget's disease (MPD) is an adenocarcinoma localized within the epidermis of the nipple and/or the areola of the breast, and it is as a rule associated with a carcinoma of the underlying lactiferous ducts, where it usually starts. MPD is relatively rare, observed in 0.7-4.3% of all breast cancers (1). We present a patient with MPD and atypical clinical finding as an annular plaque. A 74-year-old Japanese woman with a past medical history of hypothyroidism presented with a 6-month history of an itching plaque on the left areola. The patient had been treated with the application of topical steroids for a duration of approximately 5 months, and showed no clinical improvement. Physical examination showed a pink plaque encircling the nipple on the left areola (Figure 1, a). The right nipple and areola appeared normal (Figure 1, b). No palpable masses were detected within either breast. A 3.5 mm punch biopsy of the skin at the 6 o'clock position of the left areola was performed. Histological examination showed single and small aggregations of atypical cells with large hyperchromatic nuclei and pale-staining, ample cytoplasm throughout the epidermis. There was a lymphocytic infiltration in the dermis (Figure 1, c). Immunohistochemical studies were positive for CK7 and negative for S-100 and HMB45. With the diagnosis of MPD, the patient underwent a partial mastectomy of the left breast center area, consisting of surgical excision of the left nipple, the adjacent surrounding areolar skin, and subcutaneous tissues. Subsequently, radiation therapy for the residual breast was prepared. As has been described in detail by Kanitakis, the skin lesion develops insidiously as a scaly, fissured, or oozing erythema of the nipple and, more rarely, the areola. Advanced lesions present as a well-demarcated, round, ovoid, or polycyclic eczema-like plaque with a pink or red hue. It is occasionally slightly infiltrated and has an erosive, oozing, scaly, or crusted surface. The lesions are almost invariably unilateral, showing centrifugal spread. Retraction or ulceration of the nipple are often noted (1). The present case exhibited a very rare clinical finding of a plaque encircling the nipple, which has not been reported previously. It was initially difficult to establish the diagnosis of MPD, and biopsy was needed to obtain a definitive diagnosis. Differential diagnosis of MPD comprises eczema as atopic dermatitis or contact dermatitis, erosive adenomatosis, and malignant skin condition such as Bowen's disease, superficial basal cell carcinoma, or superficially spreading melanoma. As in the present case, individuals presenting with an annular plaque are often considered to have sebaceous hyperplasia. Sebaceous hyperplasia is a common, benign skin condition involving hypertrophy of the sebaceous glands, common in middle-aged or older adults (2). These lesions can be single or multiple and manifest as yellow, soft, small papules. These papules are occasionally seen around the nipple, forming an annular plaque. In general, sebaceous hyperplasia is described as yellow-colored papules among Caucasians. However, caution is needed, since it is characterized by skin-colored papules among some Asians.In the present case, some pigmentation (2 to 3 mm in diameter) was observed on the left nipple. Pigmented MPD have been reported, and the mechanism underlying the pigmentation is not yet fully understood, but it has been proposed that Paget cells may release melanocytic chemoattractants or basic fibroblast growth factors that stimulate the proliferation of melanocytes within the tumor nests (3). The possibility of physiological pigmentation cannot be ruled out in the present case; on the other hand, the possibility of pigmented MPD cannot be ruled out either, since no pigmentation was observed on the right nipple.
乳腺佩吉特病(MPD)是一种局限于乳头和/或乳晕表皮的腺癌,通常与乳腺导管内癌相关,且往往起源于此。MPD相对罕见,在所有乳腺癌中占0.7 - 4.3%(1)。我们报告一例患有MPD且临床表现为环形斑块的非典型病例。
一名74岁的日本女性,有甲状腺功能减退病史,左侧乳晕出现瘙痒斑块6个月。患者外用类固醇治疗约5个月,未见临床改善。体格检查发现左侧乳晕有一个粉红色斑块环绕乳头(图1,a)。右侧乳头和乳晕外观正常(图1,b)。双侧乳房均未触及肿块。在左侧乳晕6点位置取3.5mm皮肤组织进行穿刺活检。组织学检查显示表皮内有单个及小簇状非典型细胞,核大、染色质深,胞质淡染且丰富。真皮层有淋巴细胞浸润(图1,c)。免疫组化研究显示CK7阳性,S - 100和HMB45阴性。诊断为MPD后,患者接受了左侧乳房中央区部分乳房切除术,包括切除左侧乳头、相邻的乳晕皮肤及皮下组织。随后准备对残留乳房进行放射治疗。
正如卡尼塔基斯详细描述的那样,皮肤病变起初表现为乳头的鳞屑状、裂隙状或渗出性红斑,乳晕处更为少见。进展期病变表现为边界清晰的圆形、椭圆形或多环状湿疹样斑块,呈粉红色或红色。偶尔有轻微浸润,表面有糜烂、渗出、鳞屑或结痂。病变几乎均为单侧,呈离心性扩散。常可见乳头回缩或溃疡(1)。本病例呈现出一种非常罕见的临床特征,即斑块环绕乳头,此前未见报道。最初很难确诊MPD,需要活检才能明确诊断。MPD的鉴别诊断包括特应性皮炎或接触性皮炎等湿疹、糜烂性腺瘤病以及恶性皮肤疾病,如鲍温病、浅表基底细胞癌或浅表扩散性黑色素瘤。如本病例所示,出现环形斑块的患者常被认为患有皮脂腺增生。皮脂腺增生是一种常见的良性皮肤疾病,表现为皮脂腺肥大,多见于中年或老年人(2)。这些病变可为单个或多个,表现为黄色、柔软的小丘疹。这些丘疹偶尔可见于乳头周围,形成环形斑块。一般来说,白种人的皮脂腺增生表现为黄色丘疹。然而,由于部分亚洲人的皮脂腺增生表现为肤色丘疹,因此需要谨慎鉴别。
本病例中,左侧乳头观察到一些色素沉着(直径2至3mm)。有色素沉着的MPD已有报道,其色素沉着的机制尚未完全明确,但有人提出佩吉特细胞可能释放黑素细胞趋化因子或碱性成纤维细胞生长因子,刺激肿瘤巢内黑素细胞的增殖(3)。本病例不能排除生理性色素沉着的可能性;另一方面,由于右侧乳头未观察到色素沉着,也不能排除有色素沉着的MPD的可能性。