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Tetsuya KOGA, Kenichi SHIBUE, Akihiko SHIMIZU, Mizuha ARIYOSHI, Shoji ...
1996 Volume 58 Issue 4 Pages
567-569
Published: August 01, 1996
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We herein describe a 73-year-old man, who developed diffuse secondary eruptions associated with allergic contact dermatitis. He had applied Astat
® lotion to his feet for tinea pedis. One week later, diffuse secondary eruptions appeared on his trunk. In this patient, the primary lesions became clinically manifest after the development of secondary eruptions. Both a patch test and a lymphocyte stimulation test to Astat
® lotion were positive. In addition, peripheral blood mononuclear cells from the patient also released IFN-
γ and IL-5 in response to stimulation with the causative drug. The possible involvement of cytokines in the development of secondary eruptions are also discussed.
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Yasunori KUSABA, Shun’ichi KOIKE, Yoshitaka YAMADA, Satoshi DEKI ...
1996 Volume 58 Issue 4 Pages
570-573
Published: August 01, 1996
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A 58-year-old Japanese woman had been suffering for three years from refractory erythema multiforme on the bilateral lower legs. In addition, she had also been suffering from internal dental fistula of the #1 true molar tooth on the left upper jaw which had been noticed before the appearence of the skin lesions on the legs. Since an association between the erythema multiforme lesions and internal dental fistula was suggested, this tooth was extracted. Thereafter, the skin lesions temporarily became exacerbated, but soon thereafter disappeared completely leaving only pigmentation. These findings indicate that in our patient, the skin lesions developed in association with the dental lesion, probably by means of a focal infection.
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Toshiko MIYATA, Atsushi YAGUCHI, Akihiko HASHIMOTO, Toshiya ASAI, Kens ...
1996 Volume 58 Issue 4 Pages
574-577
Published: August 01, 1996
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Toxic epidermal necrolysis by omeprazole is described. A 78-year-old man developed generalized erythema over the skin and erosion on both the oral and genital mucosa 25 days after taking omeprazole for the treatment of a gastric ulcer. Nikolsky phenomenon was positive. A histological examination showed complete epidermal necrosis in bullous lesion with a sparse perivascular mononuclear cell infiltrate. He was treated with intravenous betamethasone, but unfortunately died from MRSA sepsis 10 days after onset. We also analyzed another 7 patients with toxic epidermal necrolysis treated at Kitasato University Hospital. One case, in which the histopathological features were similar to this case, also died from sepsis. The other 6 cases all survived and histopathologically showed a lichenoid tissue reaction with many necrotic keratinocytes. Based on our findings, we thus conclude that the prognosis of toxic epidennal necrolysis might therefore be related to the degree of epidermal damage and the management of bacterial infection.
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Tadashi KINOSHITA, Tomomichi ONO
1996 Volume 58 Issue 4 Pages
578-580
Published: August 01, 1996
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A case of 25-year-old male with pustular vasculitis was reported. The patient presented with many sterile pustules on erythematous plaque which were scattered over his entire body, in addition to general symptoms including fatigue and fever. Histopathologically, pustular formations in the epidermis and vasculitis in the dermis were observed. The clinical symptons including eruptions improved after the intravenous administration of corticosteroid. Thereafter, no recurrence of either the eruptions or general symptoms was observed. In addition to the pustular vasculitis, acute colitis caused by methicillin resistant
Staphylococcus aureus (MRSA) was also involved. The oral administration of minocyclin proved to be effective for this infectious disease. It was thus suggested by his clinical course that colitis by MRSA might therefore be related to the occurrence of pustular vasculitis.
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Tatsurou TANAKA, Haruhiko OHTUBO, Yutaka NARISAWA, Hiromu KOHDA
1996 Volume 58 Issue 4 Pages
581-583
Published: August 01, 1996
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We report a case of neonatal pemphigus. A female infant was born to a 37-year-old gravida 1, para 0 mother who had been regularly treated for pemphigus vulgaris for the past 13 years. In the 2 years prior to the birth, she had been well controlled with predonisone, 15 mg daily. After becoming pregnant, the mother developed erosive lesions in her mouth and on her trunk. The infant also had bullous lesions on her extremities and also showed low titers of epidemal intercellular antibodies in her sera. The skin lesions resolved within 2 weeks, but the pemphigus antibody continued to be positive for 2.5 years.
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Yuko OHNISHI, Koji HASHIMOTO
1996 Volume 58 Issue 4 Pages
584-587
Published: August 01, 1996
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We report three cases of bullous pemphigoid treated with minocyclin and niacinamide without oral corticosteroid. All three patients showed a marked improvement. Minocyclin appeared to be more effective than niacinamide in treating these case. Minocyclin therapy is therefore considered to be the first choice of treatment for bullous pemphigoid.
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Takehito ISHIKAWA, Masako MURATA, Kazue NISHIOKA, Chizuko ISHIKAWA
1996 Volume 58 Issue 4 Pages
588-592
Published: August 01, 1996
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A case of pemphigoid nodularis is reported. A 42-year-old woman with an 11-year history of pruritic prurigo nodularis-like eruptions on her trunk and extremities developed annular edematous erythema on her thighs and pea-sized tense blisters on her soles. Direct immunofluorescence studies of a prurigo nodularis-like lesion and peribullous skin showed the deposition of IgG and C3 in a linear pattern at the basement membrane zone. Indirect immunofluorescence studies revealed IgG circulating anti-basement membrane zone antibodies. Systemic examinations did not reveal any association with internal malignancies. The systemic administration of cyclosporin A and predonisolone proved to be effective in treating these prurigo nodularis-like eruptions.
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Fumiaki SHIRASAKI, Yuji YAMAGISHI, Norio OHTSUKI
1996 Volume 58 Issue 4 Pages
593-597
Published: August 01, 1996
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A case of systemic sclerosis with firm cutaneous nodules and large plaque lesions on the trunk is reported. A 53-year-old woman noted swelling in her fingers, along with arthralgia and Raynaud’s phenomenon at the age of 49. Several firm nodules and large annular plaques with severe itching had also appeared in the one year period before consultation. Physical examination revealed proximal scleroderma on the forearms, painful ulcers on the fingertips and periungual teleangiectases. Firm nodules ranging from 10∼15mm diameter in size and reddish brown, firm, annular plaques were also observed on her trunk. The largest plaque measured 110×40mm in size. A laboratory examination showed positive for anti-nuclear, anti-RNP, anti-Sm, anti-SS-A, and anti-thyroglobulin antibodies. A biopsy specimen from the plaque revealed a thickened dermis with a fibrous proliferation. In addition, an increased number of fibroblastic cells and disoriented collagen bundles were observed. We thus considered the patient’s unusually large plaques to be a rare manifestation of nodular scleroderma.
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Kyoko HATTORI, Yoshitaka HAGARI, Motoyuki MIHARA, Michiko NORIMOTO
1996 Volume 58 Issue 4 Pages
598-600
Published: August 01, 1996
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We report a 76-year-old Japanese woman who presented with Laugier-Hunziker syndrome. She had widespread, reticular, brown-black macules on the mucous membrane of the mouth and the lip and several slate-brown pigmented spots scattered on her tongue. In addition, all her fingernails had one or more longitudinal pigmented bands. There was no intestinal polyposis or adrenal dysfunction which would have suggested the presence of Peutz-Jeghers syndrome or Addison’s disease, respectively. A biopsy of a pigmented macule of the lip revealed hyperpigmentation in the basal layer with a normal number of melanocytes, thus indicating an increased production of melanin in melanocytes of the pigmented lesions.
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Yasunobu HIBI, Hiroki ONO, Chihiro HIOKI
1996 Volume 58 Issue 4 Pages
601-603
Published: August 01, 1996
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We describe a reconstruction case using a scalping flap after undergoing a wide excision of a malignant skin tumor on the nose. In this report we emphasize both the successful results of this case and technical application.
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Report of a Case Which Developed after Prostatic Carcinoma and was Followed by Hepatocellular Carcinoma
Sakae HONDA, Eiichi KAKIZOE, Shun’ichi KOIKE, Joji JIDOI, Satosh ...
1996 Volume 58 Issue 4 Pages
604-607
Published: August 01, 1996
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A 65-year-old Japanese man developed genital Paget’s disease four years after undergoing an operation for prostatic carcinoma. Estramustine phosphate sodium (Estracyt
®, 4 cap/day) had been administered to him as adjuvant chemotherapy for the prostatic carcinoma. Furthermore, he was also found to have hepatocellular carcinoma one year after the operation for genital Paget’s disease. Since both estrogen and nitrogen mustard, which are contained in estramustine phosphate sodium, are possible carcinogens, estramustine phosphate sodium is thus considered to have possibly induced genital Paget’s disease and hepatocellular carcinoma.
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Tomiko YAMAGUCHI, Kazumoto KATAGIRI, Toshihiro SATOU, Hiroto TERASHI, ...
1996 Volume 58 Issue 4 Pages
608-611
Published: August 01, 1996
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A 70-year-old woman presented with well-defined erythematous plaques and several nodules on her scalp which first developed three months previously after a minor trauma from a comb. X-ray studies and a CT scan did not reveal any metastatic lesions. The tumorous lesions were resected after a local injection of rIL-2. Although an intra-arterial injection of rIL-2 through the temporal artery given for over six months caused a gradual disappearance of the erythematous plaques, another tumor later developed on the occipital area. Therefore, instead of rIL-2, an intra-arterial injection of 5-FU and CYVADIC chemotherapy were administered. For the newly developed tumor, radiotherapy of 100Gy, using 6 MeV electrons, was given on the whole scalp. These treatments resulted in a complete remission over the three year period of treatment. The serum levels of endothelin and factor VIII-related antigen closely paralleled the size of the tumorous lesion, and continued to be relatively high even after the tumorous lesions disappeared as a result of radiotherapy.
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Yuichi YOSHIDA, Hiromaro KIRYU, Shonosuke NAGAE
1996 Volume 58 Issue 4 Pages
612-614
Published: August 01, 1996
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A 47-year-old female had a small nodule on her right upper chest since birth, which thereafter gradually increased in size. On her first visit to our hospital, a large hanging mass measured 11×9×2.5cm was observed, while adjacent to it a small café-au-lait spot-like macule was also seen. Histopathologically, the tumor exhibited the features of neurofibroma. Initially, von Recklinghausen’s disease was suspected, but the diagnosis could not be proven due to the absence of any family history or other clinical and diagnostic features. Since this case also failed to meet the diagnostic definitions of either neurofibromatoses or the “mosaic” variant of von Recklinghausen’s disease, the diagnosis of “solitary giant hanging neurofibroma” was thus considered to be most appropriate.
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Michio SASAKI, Toshihiko NUMAHARA, Kazue SASAKI, Masayoshi NISHIMOTO, ...
1996 Volume 58 Issue 4 Pages
615-618
Published: August 01, 1996
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A 77-year-old woman with scrofuloderma who had a past history of pleurisy and suspected intestinal tuberculosis at the age of 30 and 70, respectively, is reported. She developed a recalcitrant ulcer and fistule on the right chest reaching the hypochondriac muscle over the old tuberculosis lesion which was detected on the chest tomography. Treatment with RFP 300 mg and INH 400 mg daily for 10 months proved effective and resulted in some residual scar formation. We also reviewed 69 cases of scrofuloderma previously reported in the Japanese dermatological literatures over the last 20 years (from 1975 to 1994) concerning the current shift of predilection age and sites.
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1996 Volume 58 Issue 4 Pages
654-658
Published: August 01, 1996
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[in Japanese], [in Japanese]
1996 Volume 58 Issue 4 Pages
659-661
Published: August 01, 1996
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1996 Volume 58 Issue 4 Pages
662-667
Published: August 01, 1996
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1996 Volume 58 Issue 4 Pages
668-675
Published: August 01, 1996
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[in Japanese]
1996 Volume 58 Issue 4 Pages
676-683
Published: August 01, 1996
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[in Japanese]
1996 Volume 58 Issue 4 Pages
684-690
Published: August 01, 1996
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1996 Volume 58 Issue 4 Pages
691-696
Published: August 01, 1996
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[in Japanese], [in Japanese]
1996 Volume 58 Issue 4 Pages
697-705
Published: August 01, 1996
Released on J-STAGE: July 12, 2011
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