Cargando…

Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report

RATIONALE: As the initial treatment of rapidly progressive interstitial lung disease (RPILD) with antimelanoma differentiation-associated gene 5 antibody (anti-MDA5 Ab)-positive dermatomyositis (DM) patients, a combination of corticosteroids, cyclophosphamide, and calcineurin inhibitor is recommende...

Descripción completa

Detalles Bibliográficos
Autores principales: Endo, Yushiro, Koga, Tomohiro, Suzuki, Takahisa, Hara, Kazusato, Ishida, Midori, Fujita, Yuya, Tsuji, Sosuke, Takatani, Ayuko, Shimizu, Toshimasa, Sumiyoshi, Remi, Igawa, Takashi, Umeda, Masataka, Fukui, Shoichi, Nishino, Ayako, Kawashiri, Shin-ya, Iwamoto, Naoki, Ichinose, Kunihiro, Tamai, Mami, Nakamura, Hideki, Origuchi, Tomoki, Kuwana, Masataka, Kawakami, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908626/
https://www.ncbi.nlm.nih.gov/pubmed/29642214
http://dx.doi.org/10.1097/MD.0000000000010436
_version_ 1783315748186226688
author Endo, Yushiro
Koga, Tomohiro
Suzuki, Takahisa
Hara, Kazusato
Ishida, Midori
Fujita, Yuya
Tsuji, Sosuke
Takatani, Ayuko
Shimizu, Toshimasa
Sumiyoshi, Remi
Igawa, Takashi
Umeda, Masataka
Fukui, Shoichi
Nishino, Ayako
Kawashiri, Shin-ya
Iwamoto, Naoki
Ichinose, Kunihiro
Tamai, Mami
Nakamura, Hideki
Origuchi, Tomoki
Kuwana, Masataka
Kawakami, Atsushi
author_facet Endo, Yushiro
Koga, Tomohiro
Suzuki, Takahisa
Hara, Kazusato
Ishida, Midori
Fujita, Yuya
Tsuji, Sosuke
Takatani, Ayuko
Shimizu, Toshimasa
Sumiyoshi, Remi
Igawa, Takashi
Umeda, Masataka
Fukui, Shoichi
Nishino, Ayako
Kawashiri, Shin-ya
Iwamoto, Naoki
Ichinose, Kunihiro
Tamai, Mami
Nakamura, Hideki
Origuchi, Tomoki
Kuwana, Masataka
Kawakami, Atsushi
author_sort Endo, Yushiro
collection PubMed
description RATIONALE: As the initial treatment of rapidly progressive interstitial lung disease (RPILD) with antimelanoma differentiation-associated gene 5 antibody (anti-MDA5 Ab)-positive dermatomyositis (DM) patients, a combination of corticosteroids, cyclophosphamide, and calcineurin inhibitor is recommended. However, some of these patients have poor prognoses despite such intensive treatment. Other more effective treatments are desired. We report the case of an anti-MDA5 Ab-positive DM patient who had developed RPILD despite intensive treatments; she was treated successfully by a short-term plasma exchange (PE). PATIENT CONCERNS: A 71-year-old Japanese woman was admitted to the rheumatology department of another hospital with progressive muscle weakness of the limbs and erythema on both upper eyelids and the fingers of both hands. She was suspected of having classical DM (CDM) based on the findings of typical skin and myositis. Although a chest computed tomography (CT) examination showed no findings of interstitial pneumonia at the first visit to the department, she newly presented interstitial pneumonia during her admission and her anti-MDA5 Ab titer was elevated. DIAGNOSES: She was diagnosed with interstitial lung disease (ILD) with anti-MDA5 Ab-positive DM. INTERVENTIONS: She was treated with 1000 mg of methyl-prednisolone pulse, 500 mg of intravenous cyclophosphamide therapy (IVCY) followed by prednisolone 40 mg/day with tapering, and oral cyclosporine 200 mg/day. However, her interstitial pneumonia worsened with increasing breathing difficulty and an increasing serum ferritin level. She was transferred to our department, and we initiated PE as an additional treatment. OUTCOMES: After the PE treatment, all laboratory findings, for example, ferritin, KL-6, and the titer of anti-MDA5 Ab showed marked improvement, and the patient's skin symptoms and active interstitial pneumonia were relieved. LESSONS: Our patient's case suggests that PE may be effective for RPILD in anti-MDA5 Ab-positive DM patients.
format Online
Article
Text
id pubmed-5908626
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-59086262018-04-30 Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report Endo, Yushiro Koga, Tomohiro Suzuki, Takahisa Hara, Kazusato Ishida, Midori Fujita, Yuya Tsuji, Sosuke Takatani, Ayuko Shimizu, Toshimasa Sumiyoshi, Remi Igawa, Takashi Umeda, Masataka Fukui, Shoichi Nishino, Ayako Kawashiri, Shin-ya Iwamoto, Naoki Ichinose, Kunihiro Tamai, Mami Nakamura, Hideki Origuchi, Tomoki Kuwana, Masataka Kawakami, Atsushi Medicine (Baltimore) 6900 RATIONALE: As the initial treatment of rapidly progressive interstitial lung disease (RPILD) with antimelanoma differentiation-associated gene 5 antibody (anti-MDA5 Ab)-positive dermatomyositis (DM) patients, a combination of corticosteroids, cyclophosphamide, and calcineurin inhibitor is recommended. However, some of these patients have poor prognoses despite such intensive treatment. Other more effective treatments are desired. We report the case of an anti-MDA5 Ab-positive DM patient who had developed RPILD despite intensive treatments; she was treated successfully by a short-term plasma exchange (PE). PATIENT CONCERNS: A 71-year-old Japanese woman was admitted to the rheumatology department of another hospital with progressive muscle weakness of the limbs and erythema on both upper eyelids and the fingers of both hands. She was suspected of having classical DM (CDM) based on the findings of typical skin and myositis. Although a chest computed tomography (CT) examination showed no findings of interstitial pneumonia at the first visit to the department, she newly presented interstitial pneumonia during her admission and her anti-MDA5 Ab titer was elevated. DIAGNOSES: She was diagnosed with interstitial lung disease (ILD) with anti-MDA5 Ab-positive DM. INTERVENTIONS: She was treated with 1000 mg of methyl-prednisolone pulse, 500 mg of intravenous cyclophosphamide therapy (IVCY) followed by prednisolone 40 mg/day with tapering, and oral cyclosporine 200 mg/day. However, her interstitial pneumonia worsened with increasing breathing difficulty and an increasing serum ferritin level. She was transferred to our department, and we initiated PE as an additional treatment. OUTCOMES: After the PE treatment, all laboratory findings, for example, ferritin, KL-6, and the titer of anti-MDA5 Ab showed marked improvement, and the patient's skin symptoms and active interstitial pneumonia were relieved. LESSONS: Our patient's case suggests that PE may be effective for RPILD in anti-MDA5 Ab-positive DM patients. Wolters Kluwer Health 2018-04-13 /pmc/articles/PMC5908626/ /pubmed/29642214 http://dx.doi.org/10.1097/MD.0000000000010436 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 6900
Endo, Yushiro
Koga, Tomohiro
Suzuki, Takahisa
Hara, Kazusato
Ishida, Midori
Fujita, Yuya
Tsuji, Sosuke
Takatani, Ayuko
Shimizu, Toshimasa
Sumiyoshi, Remi
Igawa, Takashi
Umeda, Masataka
Fukui, Shoichi
Nishino, Ayako
Kawashiri, Shin-ya
Iwamoto, Naoki
Ichinose, Kunihiro
Tamai, Mami
Nakamura, Hideki
Origuchi, Tomoki
Kuwana, Masataka
Kawakami, Atsushi
Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report
title Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report
title_full Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report
title_fullStr Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report
title_full_unstemmed Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report
title_short Successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-MDA5 antibody-positive dermatomyositis: A case report
title_sort successful treatment of plasma exchange for rapidly progressive interstitial lung disease with anti-mda5 antibody-positive dermatomyositis: a case report
topic 6900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908626/
https://www.ncbi.nlm.nih.gov/pubmed/29642214
http://dx.doi.org/10.1097/MD.0000000000010436
work_keys_str_mv AT endoyushiro successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT kogatomohiro successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT suzukitakahisa successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT harakazusato successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT ishidamidori successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT fujitayuya successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT tsujisosuke successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT takataniayuko successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT shimizutoshimasa successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT sumiyoshiremi successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT igawatakashi successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT umedamasataka successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT fukuishoichi successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT nishinoayako successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT kawashirishinya successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT iwamotonaoki successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT ichinosekunihiro successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT tamaimami successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT nakamurahideki successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT origuchitomoki successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT kuwanamasataka successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport
AT kawakamiatsushi successfultreatmentofplasmaexchangeforrapidlyprogressiveinterstitiallungdiseasewithantimda5antibodypositivedermatomyositisacasereport