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1.
Indian J Dermatol Venereol Leprol ; 2008 Jul-Aug; 74(4): 357-60
Article in English | IMSEAR | ID: sea-53013

ABSTRACT

BACKGROUND: Several modalities of treatment have been tried in vitiligo with varied results; however, Indian data on comparative studies of two or more therapies are limited. AIMS: We compared different phototherapy methods with an oral steroid as an adjunct to determine the method with the best tolerability and efficacy. METHODS: Eighty-six patients with progressive vitiligo were randomly assigned to different study groups according to a continuous selection method over a period of one year. Group 1 was given OMP + PUVA, group 2 OMP + UVB (NB), group 3 OMP + UVB (BB) and group 4 was given OMP alone. Each patient was followed up for six months and then released from treatment. Clinical evaluation was made at the end of three and six months. RESULTS: In group 1 (OMP + PUVA), marked improvement was seen in 18.51% while moderate improvement was seen in 66.66% of the patients. Marked improvement was seen in 37.03% in group 2 (OMP + NB-UVB) while 44.44% had moderate improvement. In group 3 (OMP + BB UVB), 8.33% showed marked improvement while moderate improvement was seen in 25% of the patients. Marked and moderate improvement was seen in 5 and 10% of group 4 (OMP) patients, respectively. CONCLUSIONS: Our study compared four treatment modalities in vitiligo patients, out of which oral minipulse of steroids (OMP) only had an adjunct value and was not very effective by itself. Narrow band UVB has a definite edge over broad band UVB and should be preferred when both options are available. NB-UVB and PUVA showed comparable efficacy.


Subject(s)
Administration, Oral , Adolescent , Adult , Child , Combined Modality Therapy , Disease Progression , Dose-Response Relationship, Drug , Drug Therapy, Combination , Humans , Middle Aged , PUVA Therapy , Steroids/administration & dosage , Treatment Outcome , Ultraviolet Therapy , Vitiligo/pathology , Young Adult
2.
Indian J Dermatol Venereol Leprol ; 2005 May-Jun; 71(3): 182-5
Article in English | IMSEAR | ID: sea-53161

ABSTRACT

Long term D-penicillamine therapy, especially when used to treat Wilson's disease has been shown to cause elastosis perforans serpiginosa, pseudoxanthoma elasticum perforans and other degenerative dermatoses. We report a 23-year-old male patient who presented with multiple firm papules, nodules over the neck, axillae, front of elbows for five years. He was a known case of Wilson's disease on long-term treatment with penicillamine for the past 12 years. The papulonodular lesions were non-tender and some were discrete while others were arranged in a circinate pattern. There was central scarring of the skin within the circinate lesions. In addition, there were several small yellowish papules on both sides of the neck which eventually became confluent to form plaques. Histopathology confirmed the diagnosis of elastosis perforans serpiginosa and pseudoxanthoma elasticum. He was treated with cryotherapy (using liquid nitrogen through cryojet) for former lesions. The lesions showed remarkable improvement after five sittings. Now the patient is under trientine hydrochloride (750 mg twice daily) for Wilson's disease.


Subject(s)
Adult , Biopsy, Needle , Cryotherapy/methods , Dose-Response Relationship, Drug , Elastic Tissue/pathology , Follow-Up Studies , Hepatolenticular Degeneration/diagnosis , Humans , Immunohistochemistry , Male , Penicillamine/adverse effects , Pseudoxanthoma Elasticum/chemically induced , Severity of Illness Index , Treatment Outcome
3.
Article in English | IMSEAR | ID: sea-95181

ABSTRACT

A case of poikiloderma developed polymyositis ten years after the onset of skin changes. This rare case of poikilodermatomyositis, hitherto not reported from Asian continent, is documented.


Subject(s)
Dermatomyositis/complications , Diagnosis, Differential , Female , Humans , Middle Aged , Polymyositis/diagnosis , Rothmund-Thomson Syndrome/complications , Time Factors
4.
Indian J Dermatol Venereol Leprol ; 2002 Nov-Dec; 68(6): 342-3
Article in English | IMSEAR | ID: sea-52473

ABSTRACT

A 23-year old man presented with firm cutaneous and subcutaneous nodules of histoid leprosy. Some of the nodules suppurated after multidrug therapy (MDT) and these nodules showed features of erythema nodosum leprosum (ENL) on histopathological examination. ENL is a rare phenomenon observed in histoid leprosy.

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