Systemic amyloidosis in a patient with adult onset still's disease

Tomonori Ishii; Takeshi Sasaki; Tai Muryoi; Chihiro Murai; Akira Hatakeyama; Hirofumi Oosaki; Akira Yusa; Kaoru Yoshinaga; Toru Kawanami

doi:10.2169/internalmedicine.32.50

Systemic amyloidosis in a patient with adult onset still's disease

Tomonori Ishii, Takeshi Sasaki, Tai Muryoi, Chihiro Murai, Akira Hatakeyama, Hirofumi Oosaki, Akira Yusa, Kaoru Yoshinaga, Toru Kawanami

Clinical Research, Innovation and Education Center

Research output: Contribution to journal › Article › peer-review

13 Citations (Scopus)

Abstract

A 39-year-old woman presented clinical features of adult onset Still's disease. Seven years after the onset, she developed renal insufficiency and biopsy studies revealed amyloid deposits involving amyloid A protein, P component, λ chain and K chain in the kidney and rectum. She died in 1992, primarily due to cardiac failure associated with amyloidosis, indicating that amyloidosis should be considered one of the fatal complications in adult onset Still's disease with a long history.

Original language	English
Pages (from-to)	50-52
Number of pages	3
Journal	Internal Medicine
Volume	32
Issue number	1
DOIs	https://doi.org/10.2169/internalmedicine.32.50
Publication status	Published - 1993

Keywords

amyloid
joint pain

ASJC Scopus subject areas

Internal Medicine

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AU - Ishii, Tomonori

AU - Sasaki, Takeshi

AU - Muryoi, Tai

AU - Murai, Chihiro

AU - Hatakeyama, Akira

AU - Oosaki, Hirofumi

AU - Yusa, Akira

AU - Yoshinaga, Kaoru

AU - Kawanami, Toru

PY - 1993

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N2 - A 39-year-old woman presented clinical features of adult onset Still's disease. Seven years after the onset, she developed renal insufficiency and biopsy studies revealed amyloid deposits involving amyloid A protein, P component, λ chain and K chain in the kidney and rectum. She died in 1992, primarily due to cardiac failure associated with amyloidosis, indicating that amyloidosis should be considered one of the fatal complications in adult onset Still's disease with a long history.

AB - A 39-year-old woman presented clinical features of adult onset Still's disease. Seven years after the onset, she developed renal insufficiency and biopsy studies revealed amyloid deposits involving amyloid A protein, P component, λ chain and K chain in the kidney and rectum. She died in 1992, primarily due to cardiac failure associated with amyloidosis, indicating that amyloidosis should be considered one of the fatal complications in adult onset Still's disease with a long history.

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Systemic amyloidosis in a patient with adult onset still's disease

Abstract

Keywords

ASJC Scopus subject areas

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