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Cavitating Lung Disease: A Novel Presentation of IgG4-Related Disease
Patient: Male, 60 Final Diagnosis: IgG4 related disease Symptoms: Cough • hemoptysis Medication: — Clinical Procedure: None Specialty: Pulmonology OBJECTIVE: Rare disease BACKGROUND: Immunoglobulin (Ig) G4-related disease, previously referred to as IgG4-related sclerosing disease or hyper-IgG4 disea...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514329/ https://www.ncbi.nlm.nih.gov/pubmed/26196118 http://dx.doi.org/10.12659/AJCR.894015 |
Sumario: | Patient: Male, 60 Final Diagnosis: IgG4 related disease Symptoms: Cough • hemoptysis Medication: — Clinical Procedure: None Specialty: Pulmonology OBJECTIVE: Rare disease BACKGROUND: Immunoglobulin (Ig) G4-related disease, previously referred to as IgG4-related sclerosing disease or hyper-IgG4 disease, may occur in the lung, involving alveolar parenchyma, airways, and pleura. Various pulmonary manifestations of IgG4-related disease have been reported, but to the best of our knowledge a cavitating lung disease has not been reported previously. CASE REPORT: We describe a 60-year-old man who presented with hemoptysis and cavitating lung disease with clinical, laboratory, and histopathologic findings compatible with IgG4-related disease. Other potential causes of cavitation were excluded. Treatment was initiated with oral prednisone and subsequently mycophenolate mofetil was added. Follow-up 1 year later shows stable pulmonary function with complete resolution of the cavitary lesions. CONCLUSIONS: We present a case of cavitating lung disease as a previously unreported manifestation of IgG4-related disease. Our patient had an excellent response to immunosuppression. An increased awareness of IgG4-related disease and its myriad of manifestations is very important for pulmonologists. |
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