Zobrazeno 1 - 10
of 39 989
pro vyhledávání: ''
Autor:
Shigeru Hayashi, Kenji Sakai, Takayuki Nojima, Masanao Mohri, Makoto Mori, Masahito Yamada, Katsuhiko Saito, Keitaro Matsubara
Publikováno v:
Internal Medicine. 61:1903-1906
We herein report a 73-year-old man with isolated hypertrophic pachymeningitis (HP) showing serological and pathological characteristics of both IgG4-related disorders and granulomatosis with polyangiitis. The patient presented with chronic onset head
Autor:
Masaki Etoh, Kanako Asai, Noriko Miyashita, Akira Nishikawa, Hisae Sumi, Akiko Yoshimura, Yasuyoshi Kimura, Akihiro Hashiguchi, Takashi Naka, Hiroshi Takashima
Publikováno v:
Internal Medicine. 61:1743-1747
Charcot-Marie-Tooth disease (CMT) is a common hereditary peripheral polyneuropathy encompassing distinct monogenetic disorders. Pathogenic mutations in mitofusin 2 (MFN2) are the most frequent cause of its axonal type, CMT type 2A, with diverse pheno
Publikováno v:
Internal Medicine. 61:1603-1608
A 41-year-old woman was diagnosed with polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome based on polyneuropathy, hepatosplenomegaly, sclerotic bone lesions, IgA-λ M-protein, and an elevated level of serum va
Publikováno v:
Internal Medicine. 61:1415-1422
A 57-year-old woman presented with optic neuritis with repeated clinical symptoms of focal demyelination of the cerebral white matter and brain stem for 14 years. At the end of the patient's course, the clinical signs mimicked secondary progressive m
Autor:
Kenichiro Narisawa, Nobuyuki Koyama, Tomoyuki Fujita, Yoshiya Katsura, Minoru Fujimori, Masahiko Kure, Terumasa Nagase, Tomoya Ishii, Yukihisa Takeda, Koichiro Kogure, Tomotada Odaka
Publikováno v:
Internal Medicine. 61:1183-1188
A 51-year-old woman was admitted because of hypercalcemia. Neck ultrasonography and computed tomography revealed the presence of parathyroid cysts on both sides. After primary hyperparathyroidism was diagnosed by technetium-99m-methoxyisobutylisonitr
Autor:
Tomohiro Tomiyasu, Tadasu Kojima, Dan Inoue, Muneharu Yamada, Shuhei Komatsu, Takahiro Uchida, Takashi Oda, Noriko Yoshikawa
Publikováno v:
Internal Medicine. 61:1021-1026
Infections with neuraminidase-producing bacteria can lead to acute kidney injury (AKI). We herein report a 74-year-old woman who developed AKI in the course of Capnocytophaga infection, a neuraminidase-producing bacterium. A renal biopsy showed tubul
Autor:
Daigo Hashimoto, Nanase Okazaki, Masahiro Onozawa, Junichi Sugita, Daisuke Hidaka, Shinichi Fujisawa, Atsushi Yasumoto, Keito Suto, Naoki Miyashita, Hiroyuki Ohigashi, Yoshihiro Matsuno, Takanori Teshima
Publikováno v:
Internal Medicine. 61:1049-1054
Right neck swelling and pain occurred in a 49-year-old man. A Blood count showed a slight increase in platelet count without leukemoid reaction. After a biopsy of the cervical mass and bone marrow aspiration, a diagnosis of extramedullary blast crisi
Autor:
Naohiro Toda, Eri Muso, Toshiyuki Komiya, Takaki Sakurai, Hisako Hirashima, Satoshi Kurahashi, Katsuhiro Io, Jun Takeoka, Masaaki Fujita, Katsuya Tanigaki
Publikováno v:
Internal Medicine. 61:1027-1032
Rosai-Dorfman-Destombes disease (RDD) is a non-Langerhans cell histiocytosis characterized by the accumulation of histiocytes inside the lymph nodes or extranodally. The association between RDD and IgG4-related disease (IgG4-RD) is discussed. We here
Autor:
Shintaro Miyamoto, Hiroshi Iwamoto, Tatsuo Ichinohe, Kazunori Fujitaka, Tomoko Koura, Noriyasu Fukushima, Hironobu Hamada, Takahiro Kambara, Koichi Ohshima, Shinjiro Sakamoto, Takeshi Masuda, Taku Nakashima, Hiroki Tanahashi, Noboru Hattori, Kyohei Yamada, Kakuhiro Yamaguchi, Yasushi Horimasu
Publikováno v:
Internal Medicine. 61:1043-1048
This is the first report describing primary pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma with the high expression of IgG4. The histological findings were compatible with the diagnostic criteria for MALT lymphoma and IgG4-related respir
Autor:
Hiroshi Ishii, Yusuke Ueda, Takuto Miyamura, Yuji Yoshida, Hisako Kushima, Mitsuharu Ueda, Takato Ikeda, Seiji Haraoka, Yoshiaki Kinoshita
Publikováno v:
Internal Medicine. 61:877-881
Amyloidosis is a rare disease characterized by the deposition of abnormal proteins in extracellular tissues. We herein report a case with instructive radiologic features of nodular pulmonary amyloidosis associated with Sjögren's syndrome. A 67-year-