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Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations
Unusual presentations of sarcoidosis pose a diagnostic challenge and warrant attention. Hematologic associations: Case 1 (37-years-old male): Pancytopenia: myelofibrosis (leading to sepsis and mortality) following a two-year quiescent course of biopsy-proven-sarcoidosis. Case 2: (38-years-old male):...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390548/ https://www.ncbi.nlm.nih.gov/pubmed/34471595 http://dx.doi.org/10.1016/j.rmcr.2021.101495 |
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author | Medhat, Basma M. Behiry, Mervat E. Fateen, Mohamed El-Ghobashy, Nehal Fouda, Raghda Embaby, Aya Seif, Esraa M. Taha, Marwa Magdy Hasswa, Mohammed Kamal Sobhy, Dina Ragheb, Christina Samir Morad, Mohamed Abdelkader |
author_facet | Medhat, Basma M. Behiry, Mervat E. Fateen, Mohamed El-Ghobashy, Nehal Fouda, Raghda Embaby, Aya Seif, Esraa M. Taha, Marwa Magdy Hasswa, Mohammed Kamal Sobhy, Dina Ragheb, Christina Samir Morad, Mohamed Abdelkader |
author_sort | Medhat, Basma M. |
collection | PubMed |
description | Unusual presentations of sarcoidosis pose a diagnostic challenge and warrant attention. Hematologic associations: Case 1 (37-years-old male): Pancytopenia: myelofibrosis (leading to sepsis and mortality) following a two-year quiescent course of biopsy-proven-sarcoidosis. Case 2: (38-years-old male): Presentation with thrombocytopenia (5 × 10(3)/cmm): immune thrombocytopenic purpura (histologically associated with megakaryocytic emperipolesis). Biopsied enlarged lymph nodes demonstrated sarcoidosis. Hematologic sarcoid involvement is usually due to granulomatous bone marrow (3.9%) or splenic infiltration (6–30%); however, the presented manifestations are scarcely reported with a potential significance that is yet to be elucidated. Case 3: Neurologic presentation: 48-years-old female: presentation with bilateral sensorineural hearing loss and facial palsy. Brain magnetic resonance imaging showed leptomeningeal thickening. Biopsied enlarged lymph nodes showed sarcoidosis. Case 4: Neurologic and renal manifestations: 13-years-old male (family history of sarcoidosis): Presenting with acute headache, investigations showed elevated serum creatinine (2.1 mg/dL) and angiotensin converting enzyme, and computed tomography chest and abdominal findings characteristic of sarcoidosis. Associated benign increased intracranial and acute tubulointerstitial nephritis (with eosinophils) were diagnosed upon concordant workup. Of sarcoidosis neurologic affection (5–10%), cranial nerve(s) involvement is among the most common (25–50% of neurosarcoid affection), particularly that of the facial nerve (Case 3). Leptomeningeal enhancement is among the most common neurosarcoid radiologic findings (30–40%). Whereas benign increased intracranial tension (Case 4) is much less reported. Among sarcoidosis renal involvement (35–50%), interstitial nephritis usually presents with granulomatous renal lesions, yet its sole association with sarcoidosis is unusual (Case 4). The portrayed atypical hematologic, neurologic, and renal manifestations further emphasize the masquerading nature of sarcoidosis. |
format | Online Article Text |
id | pubmed-8390548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83905482021-08-31 Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations Medhat, Basma M. Behiry, Mervat E. Fateen, Mohamed El-Ghobashy, Nehal Fouda, Raghda Embaby, Aya Seif, Esraa M. Taha, Marwa Magdy Hasswa, Mohammed Kamal Sobhy, Dina Ragheb, Christina Samir Morad, Mohamed Abdelkader Respir Med Case Rep Case Report Unusual presentations of sarcoidosis pose a diagnostic challenge and warrant attention. Hematologic associations: Case 1 (37-years-old male): Pancytopenia: myelofibrosis (leading to sepsis and mortality) following a two-year quiescent course of biopsy-proven-sarcoidosis. Case 2: (38-years-old male): Presentation with thrombocytopenia (5 × 10(3)/cmm): immune thrombocytopenic purpura (histologically associated with megakaryocytic emperipolesis). Biopsied enlarged lymph nodes demonstrated sarcoidosis. Hematologic sarcoid involvement is usually due to granulomatous bone marrow (3.9%) or splenic infiltration (6–30%); however, the presented manifestations are scarcely reported with a potential significance that is yet to be elucidated. Case 3: Neurologic presentation: 48-years-old female: presentation with bilateral sensorineural hearing loss and facial palsy. Brain magnetic resonance imaging showed leptomeningeal thickening. Biopsied enlarged lymph nodes showed sarcoidosis. Case 4: Neurologic and renal manifestations: 13-years-old male (family history of sarcoidosis): Presenting with acute headache, investigations showed elevated serum creatinine (2.1 mg/dL) and angiotensin converting enzyme, and computed tomography chest and abdominal findings characteristic of sarcoidosis. Associated benign increased intracranial and acute tubulointerstitial nephritis (with eosinophils) were diagnosed upon concordant workup. Of sarcoidosis neurologic affection (5–10%), cranial nerve(s) involvement is among the most common (25–50% of neurosarcoid affection), particularly that of the facial nerve (Case 3). Leptomeningeal enhancement is among the most common neurosarcoid radiologic findings (30–40%). Whereas benign increased intracranial tension (Case 4) is much less reported. Among sarcoidosis renal involvement (35–50%), interstitial nephritis usually presents with granulomatous renal lesions, yet its sole association with sarcoidosis is unusual (Case 4). The portrayed atypical hematologic, neurologic, and renal manifestations further emphasize the masquerading nature of sarcoidosis. Elsevier 2021-08-21 /pmc/articles/PMC8390548/ /pubmed/34471595 http://dx.doi.org/10.1016/j.rmcr.2021.101495 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Medhat, Basma M. Behiry, Mervat E. Fateen, Mohamed El-Ghobashy, Nehal Fouda, Raghda Embaby, Aya Seif, Esraa M. Taha, Marwa Magdy Hasswa, Mohammed Kamal Sobhy, Dina Ragheb, Christina Samir Morad, Mohamed Abdelkader Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations |
title | Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations |
title_full | Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations |
title_fullStr | Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations |
title_full_unstemmed | Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations |
title_short | Sarcoidosis beyond pulmonary involvement: A case series of unusual presentations |
title_sort | sarcoidosis beyond pulmonary involvement: a case series of unusual presentations |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390548/ https://www.ncbi.nlm.nih.gov/pubmed/34471595 http://dx.doi.org/10.1016/j.rmcr.2021.101495 |
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