Treatment of Desquamative Interstitial Pneumonia and Systemic Sclerosis with Corticosteroids and Immunosuppressants

A 66-year-old male ex-smoker presented with fatigue and non-productive cough, as well as a 2-year history of ground-glass opacities. Deterioration on chest radiography and increased Krebs von den Lungen-6 levels coincided with the progression of diffuse ground-glass opacities on high-resolution computed tomography. Surgical lung biopsy revealed features consistent with desquamative interstitial pneumonia. Concurrent skin hardening and presence of anti-Scl-70 antibodies supported the diagnosis of systemic sclerosis. Treatment with oral corticosteroids proved to be effective, leading to radiographic improvement. The subsequent administration of cyclophosphamide and mycophenolate mofetil stabilized disease progression.

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Publication Details

Journal
Internal Medicine
Published
2025-04-04
DOI
https://doi.org/10.2169/internalmedicine.5001-24
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
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article

Treatment of Desquamative Interstitial Pneumonia and Systemic Sclerosis with Corticosteroids and Immunosuppressants

Satoshi Goshima, Ruriko Asahi, Mariko Asano, S. Sakamoto et al.
Internal Medicine
Systemic Sclerosis and Related Diseases
article

Treatment of Desquamative Interstitial Pneumonia and Systemic Sclerosis with Corticosteroids and Immunosuppressants

Satoshi Goshima, Ruriko Asahi, Mariko Asano, S. Sakamoto, Masahide Takeda, Yūji Okuda, Katsutoshi Nakayama, Yuri Takita, Yuka Izumiya, Kentaroh Kudoh, Daisuke Takahashi, Kazuhiro Sato, Kengo Shimada, Eiki Omoto
article en

Abstract

A 66-year-old male ex-smoker presented with fatigue and non-productive cough, as well as a 2-year history of ground-glass opacities. Deterioration on chest radiography and increased Krebs von den Lungen-6 levels coincided with the progression of diffuse ground-glass opacities on high-resolution computed tomography. Surgical lung biopsy revealed features consistent with desquamative interstitial pneumonia. Concurrent skin hardening and presence of anti-Scl-70 antibodies supported the diagnosis of systemic sclerosis. Treatment with oral corticosteroids proved to be effective, leading to radiographic improvement. The subsequent administration of cyclophosphamide and mycophenolate mofetil stabilized disease progression.

Internal MedicineVol. 64(20)
Akita University (JP)
Good health and well-being
Openalex Percentile: Top 90%
Systemic Sclerosis and Related Diseases
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