1.A case of scar sarcoidosis.
Young Chul HONG ; Dong Jib NA ; Sang Hoon HAN ; Yang Deok LEE ; Yong Seon CHO ; Min Soo HAN
The Korean Journal of Internal Medicine 2008;23(4):213-215
Infiltration of sarcoid granuloma in old cutaneous scars is one of the uncommon cutaneous manifestations of sarcoidosis. Here, we report the case of a 47-year-old female who presented with swelling and irritation in 5 old scars. She had acquired these scars 9 years ago in a traffic accident. An incisional scar biopsy revealed noncaseating granulomas consistent with sarcoidosis. High-resolution CT (HRCT) revealed right paratracheal, both hilar, paraaortic, and subcarinal lymphadenopathy without any nodular densities in both lung fields. Successful regression of cutaneous inflammation was achieved using a short course of oral steroids.
Cicatrix/*pathology
;
Female
;
Humans
;
Middle Aged
;
Sarcoidosis/*diagnosis/therapy
;
Skin Diseases/*diagnosis/therapy
2.A case report of childhood hematidrosis.
Li-Jun WANG ; Cai-Xia AN ; Yu-Mei LI ; Chang-Qing CAO
Chinese Journal of Contemporary Pediatrics 2014;16(2):214-215
Female
;
Hemorrhage
;
diagnosis
;
therapy
;
Humans
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Infant
;
Skin Diseases
;
diagnosis
;
therapy
;
Sweat
3.Large subcutaneous calcification in systemic lupus erythematosus: treatment with oral aluminum hydroxide administration followed by surgical excision.
Young Min PARK ; Sang Jung LEE ; Hoon KANG ; Sang Hyun CHO
Journal of Korean Medical Science 1999;14(5):589-592
A 32-year-old woman with a long-standing systemic lupus erythematosus had multiple subcutaneous nodules on her axillae, iliac crests and limbs. Three years ago, these nodules began to appear and slowly became larger. Some of them amassed to form a large, fungating, lobulated mass on her right iliac crest. Roentgenographic and histological examination showed that they were calcium deposits. She was initially treated with aluminum hydroxide administration for nine months, which resulted in moderate decrease in size and softening in consistency, but not complete resolution. Then, the mass on the right iliac crest was excised, with an excellent early result.
Administration, Oral
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Adult
;
Aluminum Hydroxide/therapeutic use*
;
Biopsy
;
Calcinosis/therapy*
;
Calcinosis/etiology
;
Calcinosis/diagnosis
;
Case Report
;
Female
;
Human
;
Lupus Erythematosus, Systemic/complications*
;
Skin Diseases/therapy*
;
Skin Diseases/etiology
;
Skin Diseases/diagnosis
4.Large subcutaneous calcification in systemic lupus erythematosus: treatment with oral aluminum hydroxide administration followed by surgical excision.
Young Min PARK ; Sang Jung LEE ; Hoon KANG ; Sang Hyun CHO
Journal of Korean Medical Science 1999;14(5):589-592
A 32-year-old woman with a long-standing systemic lupus erythematosus had multiple subcutaneous nodules on her axillae, iliac crests and limbs. Three years ago, these nodules began to appear and slowly became larger. Some of them amassed to form a large, fungating, lobulated mass on her right iliac crest. Roentgenographic and histological examination showed that they were calcium deposits. She was initially treated with aluminum hydroxide administration for nine months, which resulted in moderate decrease in size and softening in consistency, but not complete resolution. Then, the mass on the right iliac crest was excised, with an excellent early result.
Administration, Oral
;
Adult
;
Aluminum Hydroxide/therapeutic use*
;
Biopsy
;
Calcinosis/therapy*
;
Calcinosis/etiology
;
Calcinosis/diagnosis
;
Case Report
;
Female
;
Human
;
Lupus Erythematosus, Systemic/complications*
;
Skin Diseases/therapy*
;
Skin Diseases/etiology
;
Skin Diseases/diagnosis
5.Clinical analysis of childhood acute generalized exanthematous pustulosis.
Jiang-Lin ZHANG ; Xiang CHEN ; Ji LI ; Hong-Fu XIE
Chinese Journal of Contemporary Pediatrics 2008;10(4):497-499
OBJECTIVETo describe the etiology, clinical features and treatment of childhood acute generalized exanthematous pustulosis (AGEP).
METHODSClinical data from 20 cases of childhood acute generalized exanthematous pustulosis from 1990 to 2008 were retrospectively reviewed.
RESULTSEighteen cases had a history of medication, including the use of penicillin (n=6), cephalosporins (n=3), sulphonamides (n=2), algopyrin (n=2), vaccines (n=2 ) and anti-cold drugs (n=3). Fever and generalized erythematous pustules were observed in all 20 cases. Histopathologic examination revealed spongiform superficial pustules and papillary edema. The patients were asked to stop taking suspected sensitizing drugs and received glucocorticoid treatment (1-2 mg/kg daily). After 3-5 days of the treatment, symptoms were improved and the dosage of glucocorticoid was gradually reduced. All patients were healed within 20 days after treatment.
CONCLUSIONSThe cause of AGEP is mainly attributed to the use of antibiotics, sulphonamides, antipyretic analgesics and vaccines in children. AGEP is characterized by fever and widespread pustular eruption of the skin. Removal of sensitizing factors and glucocorticoid administration is important in the treatment of AGEP in children.
Child ; Child, Preschool ; Drug Eruptions ; diagnosis ; etiology ; therapy ; Exanthema ; diagnosis ; etiology ; therapy ; Female ; Humans ; Male ; Prognosis ; Retrospective Studies ; Skin Diseases, Vesiculobullous ; diagnosis ; etiology ; therapy
6.Cutaneous sarcoidosis.
Ruifeng JI ; Mariko S Y KOH ; Louis B IRVING
Annals of the Academy of Medicine, Singapore 2007;36(12):1044-1057
7.Oral Azithromycin for Treatment of Intractable Rosacea.
Jae Hong KIM ; Yoon Seok OH ; Eung Ho CHOI
Journal of Korean Medical Science 2011;26(5):694-696
Rosacea is a common chronic cutaneous disorder that primarily occurs on the convex surfaces of the central face and is often characterized by exacerbations and remissions. A case of a 52-yr-old woman visited our clinic in February 2008 complaining typical features of rosacea including multiple pinhead to rice-sized erythematous papules. We applied various conventional treatments including topical benzoyl peroxide and metronidazole as well as oral metronidazole, isotretinoin, and doxycycline. The lesions were not controlled but were rather aggravated by complications from these treatments. Therefore, we prescribed oral azithromycin, which has anti-inflammatory effects and reduces reactive oxygen species. Ten weeks after the administration of oral azithromycin, 500 mg per day for 2 weeks, the lesions had mostly disappeared and no specific side effects related to the azithromycin were noted. Oral azithromycin dosing 500 mg/day for 2 weeks is effective for treatment of intractable rosacea.
Administration, Oral
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Azithromycin/administration & dosage/pharmacology/*therapeutic use
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Erythema/diagnosis/drug therapy
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Female
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Humans
;
Middle Aged
;
Reactive Oxygen Species
;
Rosacea/diagnosis/*drug therapy
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Skin Diseases/drug therapy
8.A Case of Herpes Zoster with Abducens Palsy.
Min Kyung SHIN ; Chun Pill CHOI ; Mu Hyoung LEE
Journal of Korean Medical Science 2007;22(5):905-907
Only a few reports have focused on ocular motor paralysis in herpes zoster ophthalmicus. We report a case of ocular motor paralysis resulting from herpes zoster. The patient, an 80-yr-old woman, presented with grouped vesicles, papules, and crusting in the left temporal area and scalp, with diplopia, impaired gaze, and severe pain. Her cerebrospinal fluid analysis was positive for varicellar zoster virus IgM. Magnetic resonance imaging was performed to rule out other diseases causing diplopia; there were no specific findings other than old infarctions in the pons and basal ganglia. Therefore, she was diagnosed of abducens nerve palsy caused by herpes zoster ophthalmicus. After 5 days of systemic antiviral therapy, the skin lesions improved markedly, and the paralysis was cleared 7 weeks later without extra treatment.
Abducens Nerve Diseases/*complications/*diagnosis/therapy
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Acyclovir/*therapeutic use
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Aged, 80 and over
;
Antiviral Agents/therapeutic use
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Female
;
Herpes Zoster/*complications/*diagnosis/therapy
;
Herpes Zoster Ophthalmicus/complications/diagnosis
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Humans
;
Skin Diseases, Viral/complications/diagnosis/therapy
;
Treatment Outcome
9.Sjogren's Syndrome.
Yonsei Medical Journal 2003;44(6):947-954
Sjogren's syndrome (SS) describes xeropthalmia and xerostomia due to lymphocytic infiltrates of lacrimal and salivary glands. SS may occur alone (primary SS) or in association with several other autoimmune diseases (secondary SS). The clinical features involve a wide variety of organs, including skin, eyes, oral cavity and salivary glands, and systems, including nervous, musculoskeletal, genitourinary and vascular. Sicca symptoms can be found in a number of other disorders including rheumatoid arthritis, systemic lupus erythematosus, scleroderma, primary biliary cirrhosis, and other rheumatic disorders.
Eye Diseases/etiology
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History of Medicine, 20th Cent.
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Human
;
Mouth Diseases/etiology
;
*Sjogren's Syndrome/complications/diagnosis/history/physiopathology/therapy
;
Skin Diseases/etiology
;
Sweden