Hypercalcaemia: A portent of sarcoidosis in cystic fibrosis

The coexistence of cystic fibrosis (CF) and sarcoidosis is rare. We report a 22-year-old male cystic fibrosis patient who presented multiple times to the Sultan Qaboos University Hospital, Muscat, Oman, in 2013. He was diagnosed with non-parathyroid-related hypercalcaemia and anterior uveitis, while...

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Main Authors: Jayakrishnan B., Saif M. Al-Mubaihsi, Masoud S. Kashoub, Jojy George
Format: Article
Language:English
Published: Sultan Qaboos University 2019-03-01
Series:Sultan Qaboos University Medical Journal
Online Access:https://journals.squ.edu.om/index.php/squmj/article/view/2999
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spelling doaj-6f5a00efb3c14e59bca82aece9a6e6c62020-11-25T03:04:35ZengSultan Qaboos UniversitySultan Qaboos University Medical Journal 2075-051X2075-05282019-03-0118453353610.18295/squmj.2018.18.04.0182538Hypercalcaemia: A portent of sarcoidosis in cystic fibrosisJayakrishnan B.0Saif M. Al-Mubaihsi1Masoud S. Kashoub2Jojy George3Department of Medicine, Sultan Qaboos University Hospital, Muscat, OmanDepartment of Medicine, Sultan Qaboos University Hospital, Muscat, OmanDepartment of Medicine, Sultan Qaboos University Hospital, Muscat, OmanDepartment of Medicine, Sultan Qaboos University Hospital, Muscat, OmanThe coexistence of cystic fibrosis (CF) and sarcoidosis is rare. We report a 22-year-old male cystic fibrosis patient who presented multiple times to the Sultan Qaboos University Hospital, Muscat, Oman, in 2013. He was diagnosed with non-parathyroid-related hypercalcaemia and anterior uveitis, while computed tomography revealed mediastinal and abdominal lymphadenopathy and mild hepatosplenomegaly. These findings, in addition to the presence of calciuria and a high angiotensin-converting enzyme (ACE) level, confirmed a clinical diagnosis of sarcoidosis. The patient responded well to treatment with oral prednisolone which, over the course of two years, resulted in the near-complete resolution of parenchymal nodular infiltrates, regression of hilar lymphadenopathy, resolution of hypercalcaemia and the normalisation of his ACE levels. Diagnosing pulmonary sarcoidosis in CF can be challenging as most adult patients already have extensive lung disease. Physicians should be aware that hypercalcaemia may be an early manifestation of sarcoidosis in such cases. Keywords: Sarcoidosis; Cystic Fibrosis; Hypercalcemia; Case Report; Oman.https://journals.squ.edu.om/index.php/squmj/article/view/2999
collection DOAJ
language English
format Article
sources DOAJ
author Jayakrishnan B.
Saif M. Al-Mubaihsi
Masoud S. Kashoub
Jojy George
spellingShingle Jayakrishnan B.
Saif M. Al-Mubaihsi
Masoud S. Kashoub
Jojy George
Hypercalcaemia: A portent of sarcoidosis in cystic fibrosis
Sultan Qaboos University Medical Journal
author_facet Jayakrishnan B.
Saif M. Al-Mubaihsi
Masoud S. Kashoub
Jojy George
author_sort Jayakrishnan B.
title Hypercalcaemia: A portent of sarcoidosis in cystic fibrosis
title_short Hypercalcaemia: A portent of sarcoidosis in cystic fibrosis
title_full Hypercalcaemia: A portent of sarcoidosis in cystic fibrosis
title_fullStr Hypercalcaemia: A portent of sarcoidosis in cystic fibrosis
title_full_unstemmed Hypercalcaemia: A portent of sarcoidosis in cystic fibrosis
title_sort hypercalcaemia: a portent of sarcoidosis in cystic fibrosis
publisher Sultan Qaboos University
series Sultan Qaboos University Medical Journal
issn 2075-051X
2075-0528
publishDate 2019-03-01
description The coexistence of cystic fibrosis (CF) and sarcoidosis is rare. We report a 22-year-old male cystic fibrosis patient who presented multiple times to the Sultan Qaboos University Hospital, Muscat, Oman, in 2013. He was diagnosed with non-parathyroid-related hypercalcaemia and anterior uveitis, while computed tomography revealed mediastinal and abdominal lymphadenopathy and mild hepatosplenomegaly. These findings, in addition to the presence of calciuria and a high angiotensin-converting enzyme (ACE) level, confirmed a clinical diagnosis of sarcoidosis. The patient responded well to treatment with oral prednisolone which, over the course of two years, resulted in the near-complete resolution of parenchymal nodular infiltrates, regression of hilar lymphadenopathy, resolution of hypercalcaemia and the normalisation of his ACE levels. Diagnosing pulmonary sarcoidosis in CF can be challenging as most adult patients already have extensive lung disease. Physicians should be aware that hypercalcaemia may be an early manifestation of sarcoidosis in such cases. Keywords: Sarcoidosis; Cystic Fibrosis; Hypercalcemia; Case Report; Oman.
url https://journals.squ.edu.om/index.php/squmj/article/view/2999
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