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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
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:
I.M. Nikishkova, V.M. Mishchenko
Publikováno v:
INTERNATIONAL NEUROLOGICAL JOURNAL. :42-47
To assess the efficacy of therapy in patients with asymptomatic brain lesions, such as «silent» brain infarcts (SBI), a number of electroencephalography (EEG) parameters can be used, as there is a correlation between EEG parameters and indices of n
Publikováno v:
La Revue de Médecine Interne. 43:26-30
Susac syndrome is a rare disease affecting mainly young women, characterized by a microangiopathy limited to the cerebral, retinal, and cochlear vessels. Although the pathophysiology of Susac syndrome is not yet fully elucidated, recent advances favo
Autor:
Masaaki Matsushima, Katsuki Eguchi, Shintaro Fujii, Azusa Nagai, Ikuko Iwata, Yuki Oshima, Ichiro Yabe, Kazuhiro Horiuchi
Publikováno v:
Internal Medicine
A 56-year-old woman presenting with type II respiratory failure was transferred to our hospital. She did not exhibit muscle weakness or elevated serum myogenic enzymes, but needle electromyography revealed myogenic changes in the limb muscles, and he
Autor:
Masahiro Tsutsumi, T. Koga, Aya Kawaguchi, Hiroaki Ida, Yumi Harada, Makiko Hayashi, Shinjiro Kaieda, Jun Akiba, Tomoaki Hoshino
Publikováno v:
Internal Medicine
We herein report an unusual case of granulomatosis with polyangiitis (GPA) in a 65-year-old man in whom relapsed disease manifested as an anterior cheek nodule. Magnetic resonance imaging indicated the differential diagnoses of the subcutaneous nodul
Autor:
Kazuhiro Murakami, Toshiharu Tabata, Motoki Kubota, Keisuke Uchida, Keigo Murakami, Yoshinobu Eishi, Naoya Ishibashi, Shuko Hata, Yasuhiro Nakamura
Publikováno v:
Internal Medicine. 60:3773-3778
We report a case of a pulmonary necrotizing sarcoid granulomatosis (NSG)-like lesion possibly associated with coinfection of Mycobacterium avium and Propionibacterium acnes. A solitary nodule in the right middle lobe of the lung was notable for coagu
Publikováno v:
INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (Ukraine). :24-27
Под наблюдением находилось 60 больных с неактивными аденомами гипофиза (НАГ). Преобладали пациенты с крупноклеточной хромофобной аденом
Autor:
Masaaki Nakayama, Koyu Suzuki, Kimio Watanabe, Kasumi Konishi, Yugo Ito, Takuya Fujimaru, Sho Fukui, Fumika Taki, Masahiko Nagahama
Publikováno v:
CEN Case Rep
A 37-year-old African–British man was referred to our hospital for detailed examination because of persistent fever, swelling and pain in both ankle joints, and blurred vision for two months. Inguinal lymph node biopsy showed a large number of epit