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Anti-PM/Scl Antibody-positive Systemic Sclerosis Complicated by Multiple Organ Involvement

A 40-year-old Japanese woman developed malignant-phase hypertension complicated by thrombotic microangiopathy, progressing to end-stage renal disease. Five years later, she was diagnosed with pulmonary arterial hypertension and interstitial pneumonia. Despite a lack of overt skin sclerosis, nucleola...

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Detalles Bibliográficos
Autores principales: Shimizu, Tatsuya, Saito, Chie, Watanabe, Megumi, Ishii, Ryota, Kawamura, Tetsuya, Nagai, Kei, Fujita, Akiko, Kaneko, Shuzo, Kai, Hirayasu, Morito, Naoki, Usui, Joichi, Yokosawa, Masahiro, Kondo, Yuya, Inoue, Sae, Okiyama, Naoko, Yamagata, Kunihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079901/
https://www.ncbi.nlm.nih.gov/pubmed/33132335
http://dx.doi.org/10.2169/internalmedicine.5665-20
Descripción
Sumario:A 40-year-old Japanese woman developed malignant-phase hypertension complicated by thrombotic microangiopathy, progressing to end-stage renal disease. Five years later, she was diagnosed with pulmonary arterial hypertension and interstitial pneumonia. Despite a lack of overt skin sclerosis, nucleolar staining in our indirect immunofluorescence analysis and nailfold capillaroscopy facilitated the diagnosis of anti-PM/Scl antibody-positive systemic sclerosis. We observed the persistent presence of anti-PM/Scl antibodies throughout the clinical course, suggesting that her kidney disease was scleroderma renal crisis. Anti-PM/Scl antibodies can be associated with multiple organ diseases. Careful attention to a patient's antinuclear antibody pattern and dermatological findings may help clarify the etiology of undiagnosed diseases.