Depew Ian, Snider William T, Cook Shane, Lim Olivia
Dermatology, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.
Cureus. 2024 Dec 18;16(12):e75948. doi: 10.7759/cureus.75948. eCollection 2024 Dec.
Cutaneous plasmacytosis (CP) is a rare condition characterized by benign proliferation of mature plasma cells in the skin. It presents as reddish-brown macules, papules, or plaques, typically located on the neck, face, and trunk. The etiology remains unknown, though it is believed to be reactive rather than malignant. CP can occasionally become systemic, affecting two or more extracutaneous organs. This report describes a 54-year-old Caucasian male patient with erythematous, scaly plaques on his lower back and arms. Histopathology revealed a dense polyclonal plasma cell infiltrate with a predominance of IgG4+ cells. The patient was treated with topical corticosteroids and referred for further systemic workup. This case emphasizes the importance of distinguishing CP from systemic plasmacytosis, which can mimic multiple myeloma, plasmacytoma, or Waldenstrom's macroglobulinemia, each requiring distinct management approaches.
皮肤浆细胞增多症(CP)是一种罕见病症,其特征为皮肤中成熟浆细胞的良性增殖。它表现为红棕色斑疹、丘疹或斑块,通常位于颈部、面部和躯干。病因尚不清楚,不过据信是反应性的而非恶性的。CP偶尔会发展为全身性,累及两个或更多皮肤外器官。本报告描述了一名54岁的白种男性患者,其下背部和手臂出现红斑鳞屑性斑块。组织病理学显示密集的多克隆浆细胞浸润,以IgG4+细胞为主。该患者接受了外用糖皮质激素治疗,并被转诊进行进一步的全身检查。该病例强调了区分CP与系统性浆细胞增多症的重要性,后者可模仿多发性骨髓瘤、浆细胞瘤或华氏巨球蛋白血症,每种情况都需要不同的管理方法。