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Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis
BACKGROUND: Sarcoidosis is a chronic disease characterized by noncaseating lesions involving any organ and tissue in the body. Hypercalcemia and acute kidney injury is a common renal presentation of sarcoidosis. Necrotizing sarcoid granulomatosis (NSG) is a granulomatous disease entity which present...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875228/ https://www.ncbi.nlm.nih.gov/pubmed/31781435 http://dx.doi.org/10.1155/2019/3736495 |
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author | Mamidi, Varun Shekar, Manikantan Chakola, Jaiju James Makkena, Vamsi Krishna Matcha, Jayakumar |
author_facet | Mamidi, Varun Shekar, Manikantan Chakola, Jaiju James Makkena, Vamsi Krishna Matcha, Jayakumar |
author_sort | Mamidi, Varun |
collection | PubMed |
description | BACKGROUND: Sarcoidosis is a chronic disease characterized by noncaseating lesions involving any organ and tissue in the body. Hypercalcemia and acute kidney injury is a common renal presentation of sarcoidosis. Necrotizing sarcoid granulomatosis (NSG) is a granulomatous disease entity which presents with nodular masses of sarcoid like granuloma which primarily effects the lungs. It is a rare necrotizing variant of sarcoidosis. Extra pulmonary presentation of NSG is very rare. CASE PRESENTATION: We present a 36-year-old female with hypercalcemia and acute kidney injury refractory to treatment. Whole body Flourine-18-fluorodeoxyglucose positron emission tomography computed tomography (18F-FDG PET/CT) showed increased metabolic uptake with ill-defined lesions in the liver, spleen, and pelvic lymph nodes. Biopsy of the ill-defined lesions in the liver showed necrotizing granulomatous lesions without angiitis. All the markers of tuberculosis were negative and angiotensin converting enzyme levels were elevated. Patient improved with 1 mg/kg/day oral steroid therapy and is on regular follow-up with minimal dose of steroids. CONCLUSION: Necrotizing sarcoid granulomatosis (NSG) is a rare systemic granulomatous disease. Due to its rarity and diagnostic difficulty, treatment is challenging for clinicians, pathologists and radiologists. Treatment of choice for symptomatic patients is steroid therapy. Prognosis is good with complete recovery. |
format | Online Article Text |
id | pubmed-6875228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-68752282019-11-28 Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis Mamidi, Varun Shekar, Manikantan Chakola, Jaiju James Makkena, Vamsi Krishna Matcha, Jayakumar Case Rep Nephrol Case Report BACKGROUND: Sarcoidosis is a chronic disease characterized by noncaseating lesions involving any organ and tissue in the body. Hypercalcemia and acute kidney injury is a common renal presentation of sarcoidosis. Necrotizing sarcoid granulomatosis (NSG) is a granulomatous disease entity which presents with nodular masses of sarcoid like granuloma which primarily effects the lungs. It is a rare necrotizing variant of sarcoidosis. Extra pulmonary presentation of NSG is very rare. CASE PRESENTATION: We present a 36-year-old female with hypercalcemia and acute kidney injury refractory to treatment. Whole body Flourine-18-fluorodeoxyglucose positron emission tomography computed tomography (18F-FDG PET/CT) showed increased metabolic uptake with ill-defined lesions in the liver, spleen, and pelvic lymph nodes. Biopsy of the ill-defined lesions in the liver showed necrotizing granulomatous lesions without angiitis. All the markers of tuberculosis were negative and angiotensin converting enzyme levels were elevated. Patient improved with 1 mg/kg/day oral steroid therapy and is on regular follow-up with minimal dose of steroids. CONCLUSION: Necrotizing sarcoid granulomatosis (NSG) is a rare systemic granulomatous disease. Due to its rarity and diagnostic difficulty, treatment is challenging for clinicians, pathologists and radiologists. Treatment of choice for symptomatic patients is steroid therapy. Prognosis is good with complete recovery. Hindawi 2019-11-05 /pmc/articles/PMC6875228/ /pubmed/31781435 http://dx.doi.org/10.1155/2019/3736495 Text en Copyright © 2019 Varun Mamidi et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Mamidi, Varun Shekar, Manikantan Chakola, Jaiju James Makkena, Vamsi Krishna Matcha, Jayakumar Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis |
title | Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis |
title_full | Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis |
title_fullStr | Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis |
title_full_unstemmed | Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis |
title_short | Acute Kidney Injury Secondary to Necrotizing Sarcoid Granulomatosis |
title_sort | acute kidney injury secondary to necrotizing sarcoid granulomatosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875228/ https://www.ncbi.nlm.nih.gov/pubmed/31781435 http://dx.doi.org/10.1155/2019/3736495 |
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