Kono Michihito, Hasegawa Tomoka, Nagai So, Odani Toshio, Akikawa Kazumasa, Nomura Yukiko, Sato Hidetsugu, Kikuchi Keisuke, Amizuka Norio, Kikuchi Hideaki
Third Department of Internal Medicine, Hokkaido P.W.F.A.C., Obihiro-Kosei General Hospital, Obihiro Department of Developmental Biology of Hard Tissue, Graduate School of Dental Medicine, Hokkaido University, Sapporo Department of Diabetes and Endocrinology, Sapporo Medical Center, NTT EC, Sapporo Division of Dermatology Division of Pathology, Hokkaido P.W.F.A.C., Obihiro-Kosei General Hospital, Obihiro, Japan.
Medicine (Baltimore). 2017 May;96(21):e6968. doi: 10.1097/MD.0000000000006968.
Palisaded neutrophilic and granulomatous dermatitis (PNGD) is a benign, inflammatory dermatosis with distinct histopathological features often observed in patients with systemic diseases. There were no reports of PNGD without underlying systemic diseases as an underlying cause of hypercalcemia. Herein, we report a case of a 62-year-old man with hypercalcemia due to PNGD, but with no underlying systemic diseases, including tuberculosis, sarcoidosis, or vasculitis.
Laboratory tests showed an elevated C-reactive protein level, an elevated corrected calcium level, a normal 25-hydroxyvitamin D level, and an elevated 1,25-dihydroxyvitamin D level. There were no other abnormalities to explain the hypercalcemia. Positron emission tomography-computed tomography showed abnormal uptake in his skin. Histopathological examination of the skin showed palisaded granulomatous infiltrate in the dermis. Neutrophils, degenerated collagen, and fibrin were present in the centers of the palisades without prominent mucin. There were no eosinophils, central necrosis, or necrotizing vasculitides. These features were consistent with PNGD.
A diagnosis of PNGD with hypercalcemia was established.
Oral prednisolone was administered to the patient.
After treatment, his symptoms resolved, and his calcium, 1,25-dihydroxyvitamin D and CRP levels returned to normal. Skin specimens before and after treatment were assessed using immunohistochemistry for 1a-hydroxylase. Granuloma and epidermal cells were 1a-hydroxylase-positive before treatment. After treatment, the granuloma diminished in size and the 1ahydroxylase-positive areas of the epidermal cells decreased.
This case was particularly unique because increased 1a-hydroxylase expression in the granuloma and epidermal cells seemed to result in hypercalcemia due to excessive transformation of 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D. Physicians should consider PNGD as an underlying cause of hypercalcemia.
栅栏状中性粒细胞和肉芽肿性皮炎(PNGD)是一种良性炎症性皮肤病,具有独特的组织病理学特征,常见于患有全身性疾病的患者。此前尚无无潜在全身性疾病作为高钙血症潜在病因的PNGD报告。在此,我们报告一例62岁男性因PNGD导致高钙血症,但无潜在全身性疾病,包括结核病、结节病或血管炎。
实验室检查显示C反应蛋白水平升高、校正钙水平升高、25-羟维生素D水平正常、1,25-二羟维生素D水平升高。无其他异常可解释高钙血症。正电子发射断层扫描-计算机断层扫描显示其皮肤有异常摄取。皮肤组织病理学检查显示真皮有栅栏状肉芽肿浸润。在栅栏中心有中性粒细胞、变性胶原和纤维蛋白,无明显粘蛋白。无嗜酸性粒细胞、中央坏死或坏死性血管炎。这些特征与PNGD一致。
确诊为伴有高钙血症的PNGD。
给患者口服泼尼松龙。
治疗后,他的症状缓解,钙、1,25-二羟维生素D和CRP水平恢复正常。使用免疫组织化学法对治疗前后的皮肤标本进行1α-羟化酶评估。治疗前肉芽肿和表皮细胞1α-羟化酶呈阳性。治疗后,肉芽肿大小减小,表皮细胞1α-羟化酶阳性区域减少。
该病例尤为独特,因为肉芽肿和表皮细胞中1α-羟化酶表达增加似乎由于25-羟维生素D过度转化为1,25-二羟维生素D而导致高钙血症。医生应考虑PNGD作为高钙血症的潜在病因。