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Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report
RATIONALE: 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 hypercal...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457875/ https://www.ncbi.nlm.nih.gov/pubmed/28538395 http://dx.doi.org/10.1097/MD.0000000000006968 |
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author | Kono, Michihito Hasegawa, Tomoka Nagai, So Odani, Toshio Akikawa, Kazumasa Nomura, Yukiko Sato, Hidetsugu Kikuchi, Keisuke Amizuka, Norio Kikuchi, Hideaki |
author_facet | Kono, Michihito Hasegawa, Tomoka Nagai, So Odani, Toshio Akikawa, Kazumasa Nomura, Yukiko Sato, Hidetsugu Kikuchi, Keisuke Amizuka, Norio Kikuchi, Hideaki |
author_sort | Kono, Michihito |
collection | PubMed |
description | RATIONALE: 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. PATIENT CONCERNS: 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. DIAGNOSES: A diagnosis of PNGD with hypercalcemia was established. INTERVENTIONS: Oral prednisolone was administered to the patient. OUTCOMES: 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. LESSONS: 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. |
format | Online Article Text |
id | pubmed-5457875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-54578752017-06-09 Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report Kono, Michihito Hasegawa, Tomoka Nagai, So Odani, Toshio Akikawa, Kazumasa Nomura, Yukiko Sato, Hidetsugu Kikuchi, Keisuke Amizuka, Norio Kikuchi, Hideaki Medicine (Baltimore) 4300 RATIONALE: 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. PATIENT CONCERNS: 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. DIAGNOSES: A diagnosis of PNGD with hypercalcemia was established. INTERVENTIONS: Oral prednisolone was administered to the patient. OUTCOMES: 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. LESSONS: 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. Wolters Kluwer Health 2017-05-26 /pmc/articles/PMC5457875/ /pubmed/28538395 http://dx.doi.org/10.1097/MD.0000000000006968 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-No Derivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 4300 Kono, Michihito Hasegawa, Tomoka Nagai, So Odani, Toshio Akikawa, Kazumasa Nomura, Yukiko Sato, Hidetsugu Kikuchi, Keisuke Amizuka, Norio Kikuchi, Hideaki Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report |
title | Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report |
title_full | Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report |
title_fullStr | Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report |
title_full_unstemmed | Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report |
title_short | Palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: A case report |
title_sort | palisaded neutrophilic and granulomatous dermatitis as a novel cause of hypercalcemia: a case report |
topic | 4300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457875/ https://www.ncbi.nlm.nih.gov/pubmed/28538395 http://dx.doi.org/10.1097/MD.0000000000006968 |
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