Refractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case report

Abstract Background Sarcoidosis is a multisystemic granulomatous disease of unknown origin. It is characterized by abnormal activation of lymphocytes and macrophages with the formation of granulomas. Most cases have asymptomatic pulmonary involvement. In case of symptoms, they have an excellent resp...

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التفاصيل البيبلوغرافية
الحاوية / القاعدة:Journal of Medical Case Reports
المؤلفون الرئيسيون: Jorge Luis Rodas Flores, Enrique Peral Gutiérrez de Ceballos, Blanca Hernández-Cruz, Alejandro Hernán Alvarez Muñoz, Jesús Machuca-Aguado, Salvador Recio Gallardo, José Javier Perez Venegas
التنسيق: مقال
اللغة:الإنجليزية
منشور في: BMC 2023-06-01
الموضوعات:
الوصول للمادة أونلاين:https://doi.org/10.1186/s13256-023-03996-w
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author Jorge Luis Rodas Flores
Enrique Peral Gutiérrez de Ceballos
Blanca Hernández-Cruz
Alejandro Hernán Alvarez Muñoz
Jesús Machuca-Aguado
Salvador Recio Gallardo
José Javier Perez Venegas
author_facet Jorge Luis Rodas Flores
Enrique Peral Gutiérrez de Ceballos
Blanca Hernández-Cruz
Alejandro Hernán Alvarez Muñoz
Jesús Machuca-Aguado
Salvador Recio Gallardo
José Javier Perez Venegas
author_sort Jorge Luis Rodas Flores
collection DOAJ
container_title Journal of Medical Case Reports
description Abstract Background Sarcoidosis is a multisystemic granulomatous disease of unknown origin. It is characterized by abnormal activation of lymphocytes and macrophages with the formation of granulomas. Most cases have asymptomatic pulmonary involvement. In case of symptoms, they have an excellent response to glucocorticoid therapy. We present a case of sarcoidosis with multi-organ involvement, refractory to multiple treatments including biological. Partial remission was achieved in it. Case presentation We report an interesting case of a 38-years-old Spanish woman treated by Heerfordt’s syndrome (uveitis, parotiditis, fever and facial palsy) plus pulmonary hiliar adenopathy. A sarcoidosis diagnosis was confirmed by lung biopsy. She was initially treated with an 8 weeks course of medium dose oral glucocorticoids and tapered over 8 weeks with improvement. After the suspension of glucocorticoids a relapse occurs with severe ocular involvement and suspicion of neurological involvement. The patient received multiple lines of treatment with poor response. Finally, after the combination of cyclophosphamide with infliximab, the uveitis resolved, improving the neurological symptoms. Conclusions Sarcoidosis is a benign disease in most cases. In a small percentage of cases behaves aggressively, requiring early diagnosis and immunosuppressive treatment to avoid sequelae. An adequate immunosuppressive therapy based on Anti TNF drugs should be started to minimize damage and improve the quality of life.The choice of treatment depends on the type and severity of the disease.
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spelling doaj-art-30e4c2e6581d48859d0bfc3287c3fda92025-08-19T22:26:08ZengBMCJournal of Medical Case Reports1752-19472023-06-011711610.1186/s13256-023-03996-wRefractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case reportJorge Luis Rodas Flores0Enrique Peral Gutiérrez de Ceballos1Blanca Hernández-Cruz2Alejandro Hernán Alvarez Muñoz3Jesús Machuca-Aguado4Salvador Recio Gallardo5José Javier Perez Venegas6Rheumatology Department, Virgen Macarena University HospitalInternal Medicine Department, Virgen Macarena University HospitalRheumatology Department, Virgen Macarena University HospitalPathological Anatomy Department, Virgen Macarena University HospitalPathological Anatomy Department, Virgen Macarena University HospitalRadiology Department, Virgen Macarena University HospitalRheumatology Department, Virgen Macarena University HospitalAbstract Background Sarcoidosis is a multisystemic granulomatous disease of unknown origin. It is characterized by abnormal activation of lymphocytes and macrophages with the formation of granulomas. Most cases have asymptomatic pulmonary involvement. In case of symptoms, they have an excellent response to glucocorticoid therapy. We present a case of sarcoidosis with multi-organ involvement, refractory to multiple treatments including biological. Partial remission was achieved in it. Case presentation We report an interesting case of a 38-years-old Spanish woman treated by Heerfordt’s syndrome (uveitis, parotiditis, fever and facial palsy) plus pulmonary hiliar adenopathy. A sarcoidosis diagnosis was confirmed by lung biopsy. She was initially treated with an 8 weeks course of medium dose oral glucocorticoids and tapered over 8 weeks with improvement. After the suspension of glucocorticoids a relapse occurs with severe ocular involvement and suspicion of neurological involvement. The patient received multiple lines of treatment with poor response. Finally, after the combination of cyclophosphamide with infliximab, the uveitis resolved, improving the neurological symptoms. Conclusions Sarcoidosis is a benign disease in most cases. In a small percentage of cases behaves aggressively, requiring early diagnosis and immunosuppressive treatment to avoid sequelae. An adequate immunosuppressive therapy based on Anti TNF drugs should be started to minimize damage and improve the quality of life.The choice of treatment depends on the type and severity of the disease.https://doi.org/10.1186/s13256-023-03996-wRefractory sarcoidosisMethotrexateAdalimumabInfliximabCase report
spellingShingle Jorge Luis Rodas Flores
Enrique Peral Gutiérrez de Ceballos
Blanca Hernández-Cruz
Alejandro Hernán Alvarez Muñoz
Jesús Machuca-Aguado
Salvador Recio Gallardo
José Javier Perez Venegas
Refractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case report
Refractory sarcoidosis
Methotrexate
Adalimumab
Infliximab
Case report
title Refractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case report
title_full Refractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case report
title_fullStr Refractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case report
title_full_unstemmed Refractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case report
title_short Refractory multisystemic sarcoidosis, a diagnosis and treatment challenge: a case report
title_sort refractory multisystemic sarcoidosis a diagnosis and treatment challenge a case report
topic Refractory sarcoidosis
Methotrexate
Adalimumab
Infliximab
Case report
url https://doi.org/10.1186/s13256-023-03996-w
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