Bullous Pemphigoid an Autoimmune Skin Disease: A Case Report
نویسندگان
چکیده
منابع مشابه
Localized genital bullous pemphigoid; A case report
Bullous pemphigoid (BP) is an autoimmune bullous disorder with urticarial pruritic papules and plaques and tense bullae in flexural surfaces of body. The localized form of the disease is a rare variant which can be triggered by different stimuli. Hereunder, we report a patient with the local type involving genitalia without any triggering factors.
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患 者:YI,68才,男 性。 主訴:全 身の浮腫. 家族歴:兄 肝臓,父 脳出血. 既往歴:25才 緑内障. 現病歴:昭 和61年8月 より前腕 と肩甲部に水 庖が出現 し全身に拡大 したため同年12月20日,本 院皮膚科に入院.12月23日 皮膚生検を施行した。 皮膚生検組織所見は図2の ごとくで真皮から表皮 が剥離 して表皮下に小水疱が形成されその部分に 好中球の浸潤がみ られ,蛍 光抗体法では皮膚基底 膜にlgGとC3の 沈着が線状にみられ,類 天庖瘡 と 診断された.ベ タメタゾン4.5mg/日 の内服で速や かに軽快 し,昭 和62年5月2日 退院 した.退 院後 もプ レ ドニゾロン10mg/日 の服用を続 けていた が,同 年12月9銭 腹痛が出現したためプレ ドニゾ Rン の内服を中止した ところ,そ の直後 より両下 肢に紅斑が出現したため12月19日 再入院 し...
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ژورنال
عنوان ژورنال: International Journal of Pharmaceutical Sciences Review and Research
سال: 2020
ISSN: 0976-044X
DOI: 10.47583/ijpsrr.2020.v65i01.024