7 results on '"Hiroko Sonoyama"'
Search Results
2. Pulmonary Thromboembolism Induced by Intravenous Immunoglobulin Therapy for Stevens-Johnson Syndrome : A Case Report
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Masutaka Furue, Maiko Ohno, Anna Hirano, Hiroko Sonoyama, Toshihiko Mashino, Takayuki Nakano, Takamichi Ito, Taketoshi Ide, and Karin Tsukamoto
- Subjects
medicine.medical_specialty ,Intravenous Immunoglobulin Therapy ,business.industry ,medicine ,Stevens johnson ,Dermatology ,business - Published
- 2019
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3. Multiple Finger and Hand Necroses Caused by Hemodialysis-associated Steal Syndrome
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Atushi Guntani, Hiroko Sonoyama, Maho Murata, Toshihiko Mashino, and Masutaka Furue
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medicine.medical_specialty ,business.industry ,Internal medicine ,medicine.medical_treatment ,Cardiology ,Medicine ,Dermatology ,Hemodialysis ,business - Published
- 2014
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4. Localization of S100A2, S100A4, S100A6, S100A7, and S100P in the human hair follicle
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Chikage, Mitoma, Futoshi, Kohda, Yukihiro, Mizote, Akira, Miake, Ayako, Ijichi, Saho, Kawahara, Miki, Kohno, Hiroko, Sonoyama, Yasutaka, Mitamura, Yumiko, Kaku, Hiroko, Inoue, Yoshiko, Sasaki, Fumitaka, Ohno, Noriko, Okabe, Nobutoshi, Take, Mika, Mizote, Akiko, Masuda, and Masutaka, Furue
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S100 Proteins ,Antibodies, Monoclonal ,Humans ,Melanocytes ,Cell Differentiation ,Immunohistochemistry ,Hair Follicle - Abstract
The hair follicle is a highly differentiated structure. In this study, we examined immunohistological localization of S100A2, S100A4, S100A6, S100A7, and S100P using specific monoclonal antibodies. S100A2 was strongly expressed in the entire outer-root sheath (ORS), but more weakly in cuticle and medulla in the bulb. S100A6, S100A7, and S100P were expressed in the innermost cells of ORS. The cuticular area was weakly positive for S100A2, S100A6, S100A7, and S100P. S100A4 was expressed in dendritic Langerhans cells and melanocytes. Sebaceous cells were variably immunopositive for S100A2, S100A6, and S100A7. A subset of dermal papilla cells expressed S100A4 and S100A6. None of the antibodies labeled the inner-root sheath. The distinct spatiostructural distributions of the S100 family proteins suggest that each protein is differentially involved in the physiological function of normal hair follicles.
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- 2014
5. Oguchi disease masked by retinitis pigmentosa
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Hidenao Ideta, Chie Ishigami, Yozo Miyake, Ryuichi Ideta, Hiroko Sonoyama, Kei Shinoda, Yumi Tada, and Masayo Takahashi
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Male ,medicine.medical_specialty ,Visual acuity ,genetic structures ,Fundus Oculi ,G-Protein-Coupled Receptor Kinase 1 ,Dark Adaptation ,Fundus (eye) ,Polymerase Chain Reaction ,Retina ,Diagnosis, Differential ,Night Blindness ,Physiology (medical) ,Ophthalmology ,Long period ,Retinitis pigmentosa ,medicine ,Ring scotoma ,Electroretinography ,Humans ,Point Mutation ,Genetic Predisposition to Disease ,Fluorescein Angiography ,Arrestin ,Blindness ,business.industry ,Oguchi disease ,Eye Diseases, Hereditary ,DNA ,Middle Aged ,medicine.disease ,eye diseases ,Sensory Systems ,Pedigree ,sense organs ,medicine.symptom ,Visual Fields ,business ,Retinitis Pigmentosa ,Tomography, Optical Coherence ,Photopic vision - Abstract
The purpose of this study was to report a patient with Oguchi disease whose ophthalmological characteristics were masked by retinitis pigmentosa (RP). The method used in this study was case report. A 53-year-old man had a progressive decrease in his visual acuity and was diagnosed with RP because of night blindness, fundoscopic findings, ring scotoma, and extinguished single-flash electroretinograms (ERGs). However, a faint golden-yellowish reflex of the retina prompted us to make a more detailed examination of the fundus after a long period of dark adaptation, ERGs, and genetic analysis. Examinations showed the Mizuo-Nakamura phenomenon, relative intact photopic ERGs, and a SAG mutation, and the patient was diagnosed with RP associated with Oguchi disease. When RP accompanies Oguchi disease, the clinical characteristics of Oguchi disease might be masked. In such a situation, the correct diagnosis is difficult. However, careful analysis of clinical findings will suggest Oguchi disease, which can be confirmed by molecular genetics.
- Published
- 2011
6. Detection of cytomegalovirus DNA from cytomegalovirus corneal endotheliitis after penetrating keratoplasty
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Shigeru Kinoshita, Shiro Amano, Hidenao Ideta, Yasuhiro Osakabe, Noriko Koizumi, Masaki Nakamura, Kaoru Araki-Sasaki, and Hiroko Sonoyama
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Ganciclovir ,Male ,medicine.medical_specialty ,Congenital cytomegalovirus infection ,Cytomegalovirus ,Eye Infections, Viral ,Antiviral Agents ,Polymerase Chain Reaction ,law.invention ,Corneal Diseases ,law ,Ophthalmology ,Cornea ,medicine ,Humans ,Polymerase chain reaction ,Immunodeficiency ,Endotheliitis ,Aged ,business.industry ,Endothelium, Corneal ,virus diseases ,Perioperative ,medicine.disease ,eye diseases ,medicine.anatomical_structure ,Cytomegalovirus Infections ,DNA, Viral ,Bullous keratopathy ,sense organs ,business ,Keratoplasty, Penetrating ,medicine.drug - Abstract
PURPOSE To report the detection of cytomegalovirus (CMV) DNA in the cornea of a CMV endotheliitis patient after penetrating keratoplasty (PKP). CASE A 71-year-old man without immunodeficiency developed corneal endotheliitis in the right eye. The patient had previously received PKP several times. Polymerase chain reaction (PCR) detected CMV-DNA in the aqueous humor in his affected eye, and we started administration of ganciclovir. There was resolution of the inflammation; however, bullous keratopathy was subsequently noted in the cornea. Additional PKP was performed with perioperative intravenous administration of ganciclovir. The failed graft obtained during the additional PKP was subjected to PCR analysis and histopathological examination. PCR analysis showed CMV-DNA in the failed graft. Little inflammatory change was noted in either the epithelial or stromal layers of the failed graft. With continued ganciclovir treatment, the graft remained clear and no recurrence or rejection occurred until 12 months after the last PKP. CONCLUSION Our PCR analysis showed the presence of CMV-DNA within the cornea of the patient with corneal endotheliitis.
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- 2010
7. Candida albicans keratitis modified by steroid application
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Hiroko Sonoyama, Tsutomu Kawasaki, Yoshitsugu Inoue, Kaoru Araki-Sasaki, Hidenao Ideta, and Nariyasu Kazama
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medicine.medical_specialty ,Pathology ,genetic structures ,medicine.medical_treatment ,Case Report ,Infectious Keratitis ,Keratitis ,Ciliary body ,Ophthalmology ,Edema ,Candida albicans ,medicine ,Abscess ,Corneal epithelium ,biology ,business.industry ,steroid ,mycotic keratitis ,cataract surgery ,RE1-994 ,Cataract surgery ,medicine.disease ,biology.organism_classification ,eye diseases ,medicine.anatomical_structure ,sense organs ,medicine.symptom ,business - Abstract
Kaoru Araki-Sasaki1, Hiroko Sonoyama1, Tsutomu Kawasaki1, Nariyasu Kazama1, Hidenao Ideta1, Yoshitsugu Inoue21Ideta Eye Hospital, Kumamoto City, Kumamoto, Japan; 2Department of Ophthalmology, Tottori University, Koyama-Minami, Tottori, Japan Abstract: The paper reports on Candida albicans ocular infection modified by steroid eye drops. A 74-year-old male complained of conjunctival injection and pain in his right eye three months after pterygium and cataract surgery. After treatment with antibiotics and steroid eye drops for three days, he was referred to our hospital. Clear localized corneal endothelial plaque with injection of ciliary body was observed. No erosion of the corneal epithelium, or infiltration of stromal edema was observed, suggesting that the pathological organism derived from the intracameral region. Because ocular infection was suspected, steroid eye drops were stopped, which led immediately to typical infectious keratitis in the pathological region, with epithelial erosion, fluffy abscess, stromal infiltration, and edema. For diagnostic purposes, the plaque was surgically removed with forceps and the anterior chamber was irrigated with antibiotics. The smear and culture examination from the plaque revealed C. albicans surrounded by neutrophils. However, aqueous fluid and fibrous tissue after gonio procedure contained no mycotic organisms. Topical fluconazole, micafungin, and pimaricin with oral itraconazole (150 mg/day) were effective. Special attention is needed when prescribing steroid eye drops to treat corneal disease especially postoperatively. Diagnosing infectious keratitis is sometimes difficult because of modification by some factors, such as postoperative conditions, scarring, and drug-induced masking. Here, we report on mycotic keratitis modified by postoperative steroid administration. Keywords: Candida albicans, cataract surgery, steroid, mycotic keratitis
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- 2009
- Full Text
- View/download PDF
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