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11. |
Annular Elastolytic Giant Cell Granuloma: An Unusual Case with Lesions Arising in Non‐sun‐exposed Areas |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 54-58
Tsutomu Muramatsu,
Toshihiko Shirai,
Yukio Yamashina,
Kuniki Sakamoto,
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摘要:
AbstractA 70‐year‐old man with a 2‐year history of annular elastolytic giant cell granuloma associated with diabetes mellitus was reported. The lesions mainly developed in non‐sun‐exposed areas. Histologic examination revealed phagocytosis of elastic fibers by histiocytic cells. Immunoperoxidase staining for lysozyme disclosed positive reactivity within the cytoplasm of these histiocytic cells. Electron microscopic study also showed elastic fibers and numerous lipid‐like substances in the cytoplasm of these cells. These findings indicate high phagocytolytic activity by these infiltrating cells. In our case, actinic damage was not considered to be a primary causative factor, and a possible pathogenesis was als
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb02996.x
年代:1987
数据来源: WILEY
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12. |
Treatment of Psoriasis Vulgaris with Oral 1α,25‐Dihydroxyvitamin D3 |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 59-62
Shigeto Morimoto,
Kunihiko Yoshikawa,
Takehito Kozuka,
Yukio Kitano,
Shunji Imanaka,
Keisuke Fukuo,
Eio Koh,
Takashi Hironaka,
Akira Zen,
Takashi Nabata,
Toshio Onishi,
Yuichi Kumahara,
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摘要:
AbstractPsoriasis is a common inflammatory skin disease, but its pathogenesis is unknown. This paper presents 2 cases of psoriasis vulgaris in which the skin lesions were improved for 3 months and more after the start of oral treatment with 1α,25‐dihydroxyvitamin D3at a dose of 0.5 μg/day. The circulating levels of calcium, inorganic phosphate, 25‐hydroxyvitamin D, 1α,25‐dihydroxyvitamin D, parathyroid hormone and calcitonin were within normal ranges before and after the start of treatment. These findings suggest that 1α,25‐dihydroxyvitamin D3has a beneficial effect on psoriatic skin lesions. It probably has a direct effect on enhancing epidermal cell differentiation.Abbreviations:Ca: calcium, hCT: calcitonin, 25‐OHD: 25‐hydroxyvitamin D, 1,25‐(OH)2D: 1α,25‐dihydroxyvitamin D, 1,25‐(OH)2D3: 1α,25‐dihydroxyvitamin D
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb02997.x
年代:1987
数据来源: WILEY
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13. |
Papulonecrotic Tuberculid |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 63-66
Chull‐Wan Ihm,
Jai‐Il Suh,
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摘要:
AbstractA case of papulonecrotic tuberculid showing widespread cutaneous eruptions is reported.
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb02998.x
年代:1987
数据来源: WILEY
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14. |
Disseminated Atypical Granuloma Annulare |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 67-69
Sándor Husz,
Éva Szabó,
János Hunyadi,
József Kohán,
Zoltán Mónus,
Nicolaus Simon,
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摘要:
AbstractGeneralized granuloma annulare commonly occurs in older adults. Atypical (perforating) forms are well known, but treatment can sometimes be complicated. A case of atypical generalized granuloma annulare successfully treated with PUVA is reported. The histology and immunohistology of the skin, histopathologic, immunohistopathologic and electronmicroscopic studies of the liver, immunoserology and laboratory investigations are detailed. The most important findings were as follows; diabetic glucose tolerance test, typical histology of the skin disease, steatosis and non‐specific reactive hepatitis, focal Kupffer cell proliferation, Kupffer cell autoantibodies in the liver and slightly enhanced liver functions. The hepatic lesions observed and latent diabetes mellitus are considered to be correlated with the generalized dermal symptom
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb02999.x
年代:1987
数据来源: WILEY
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15. |
Reactive Perforating Collagenosis |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 70-72
Krishan Kumar Bhatia,
Satish Kumar,
Anju Narang,
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摘要:
AbstractA case of reactive perforating collagenosis (RPC) is presented. The lesions appeared in a female at the age of 4 years. So far, the patient has had only two episodes of RPC and both were precipitated by cold weather. The lesions showed the Koebner phenomenon. Histological sections showed the changes of “transepidermal elimination of necrobiotic connective tissue
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb03000.x
年代:1987
数据来源: WILEY
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16. |
Localized Pemphigoid |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 73-76
Kumiko Sugihara,
Satoshi Dekio,
Kimiko Tohgi,
Joji Jidoi,
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摘要:
AbstractIn this paper, we describe a 69‐year‐old Japanese woman with localized pemphigoid. Direct immunofluorescence study showed linear IgG, IgA and C3 deposits at the basement membrane zone (BMZ). In the serum, circulating anti‐BMZ antibodies of both IgG and IgA classes were found. This is the first report of a patient with localized pemphigoid in whom circulating anti‐BMZ antibodies of not only the IgG class, but also of the IgA class were
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb03001.x
年代:1987
数据来源: WILEY
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17. |
Surgical Treatment of a Deep Fungal Infection of the Skin byTrichosporon cutaneum |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 77-80
Yoshihito Seki,
Fujio Otsuka,
Kuniaki Ohara,
Kiyohiro Takizawa,
Yasumasa Ishibashi,
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摘要:
AbstractWe treated a patient with facial granuloma caused byTrichosporon cutaneum, in whom various therapeutic modalities had been ineffective. A surgical procedure combining excision, topical chemotherapy of the open wound, and covering the defect with a cervicofacial flap was finally successful.
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb03002.x
年代:1987
数据来源: WILEY
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18. |
An Epithelioma with Hair Follicle and Apocrine Differentiation |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 81-84
Toshiki Masuda,
Jirô Arata,
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摘要:
AbstractA tumor on the face showing follicular and apocrine differentiation is described. The coexistence of the two features suggests that the hair follicle has the potential to develop an apocrine gland tumor.
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb03003.x
年代:1987
数据来源: WILEY
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19. |
Primary Osteoma Cutis |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 85-88
Shinichi Nakamura,
Toshiya Imai,
Keiji Nakayama,
Shutaro Onda,
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摘要:
AbstractA 13‐month‐old male infant with primary osteoma cutis was reported. There was no diagnostic sign of Albright's hereditary osteodystrophy in either this patient or his family. Laboratory investigations showed no abnormalities except moderate obesity (kaup index=
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb03004.x
年代:1987
数据来源: WILEY
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20. |
Solitary Angiokeratoma Seen in a Patient with Pretibial Epidermolysis Bullosa |
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The Journal of Dermatology,
Volume 14,
Issue 1,
1987,
Page 89-91
Manabu Maeda,
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摘要:
AbstractSolitary angiokeratoma was observed on the right leg of a 50‐year‐old Japanese female. In her childhood, she had repeatedly developed vesicles on the legs, and a possible diagnosis of pretibial epidermolysis bullosa was made, based on additional findings. Clinically, the condition resembled malignant melanoma and basal cell epithelioma. Possibly repeated injuries predisposed her to the development of solitary angiokerat
ISSN:0385-2407
DOI:10.1111/j.1346-8138.1987.tb03005.x
年代:1987
数据来源: WILEY
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