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Citation statistics : Table of Contents
2012| May-August | Volume 3 | Issue 2
Online since
May 29, 2012
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CASE REPORTS
Coexistence of psoriasis with bullous pemphigoid
Raghavendra Rao, Akash Gupta, Fousiya Yunis, Sripathi Handettu, Balachandran Chandrashekar
May-August 2012, 3(2):119-121
DOI
:10.4103/2229-5178.96707
PMID
:23130285
Psoriasis vulgaris and bullous pemphigoid (BP) represent two clinically well-characterized, chronic, inflammatory skin conditions. The concomitant occurrence of these two entities in a patient is rare. Here we report a 57-year-old male suffering from psoriasis vulgaris for 15 years on irregular medication who noticed eruption of blisters all over the body. We believe that this is the first case report of psoriasis vulgaris coexistent with bullous pemphigoid in Indian literature. Please check where you want bullous pemphigoid and where you want psoriasis pemphigoides.
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ORIGINAL ARTICLES
Clinical patterns of vitiligo and its associated co morbidities: A prospective controlled cross-sectional study in South India
DS Krupa Shankar, K Shashikala, Rama Madala
May-August 2012, 3(2):114-118
DOI
:10.4103/2229-5178.96705
PMID
:23130284
Aim:
The purpose of this study is to assess the clinical patterns and associations of vitiligo, audiometric functions, and ocular involvement and to correlate the morphology, clinical behaviour and comorbidities associated with vitiligo.
Settings and Design:
For this prospective and cross-sectional study 80 self-reporting patients in the age group 7-75 years with vitiligo attending the outpatient department of Manipal hospital during the period August 2008 to February 2010 were selected and the data was analysed.
Materials and Methods:
The patients were subjected to detailed history, clinical examination and investigations [complete blood count (CBC), absolute eosinophil count (AEC), erythrocyte sedimentation rate (ESR), thyroid stimulating hormone (TSH), vitamin B12 estimation, fasting blood sugar (FBS), and post prandial blood sugar (PPBS),antibody titre estimations that is antithyroid peroxidase (ATPA), antithyroglobulin (ATA), antinuclear antibodies (ANA),urine analysis], audiometric evaluation and ophthalmic examination.
Statistical Analysis Used:
The Fisher exact test has been used to find the significance of study parameters on categorical scale between two or more groups.
Results:
In the present series of 80 cases, 41 (51.25%) were males and 39 (48.75%) were females. The male to female ratio was 1.05:1. In our study 20% cases gave definite family history of vitiligo and patients in the age group of 20 - 30 years were the most commonly affected. Generalized vitiligo (31.3%) was the most common type followed by segmental (30%), focal (18.8%), acrofacial (8.8%), and mucosal vitiligo (11.3%). In the present study there was a high incidence of autoantibodies (22.5%), vitamin B12 deficiency (30%), hypothyroidism (11.3%), elevated absolute eosinophil count (16.3%), hypoacusis (10%) and retinal changes (8.8%). This suggests multisystem autoimmunity in vitiligo.
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REVIEW ARTICLES
Oral cavity and leprosy
Shambulingappa Pallagatti, Soheyl Sheikh, Anupreet Kaur, Amit Aggarwal, Ravinder Singh
May-August 2012, 3(2):101-104
DOI
:10.4103/2229-5178.96700
PMID
:23130281
Although leprosy involves the oral cavity in up to 60% of the patients, examination of the oral cavity in leprosy clinics or oral health science clinics is often neglected. Oral involvement in leprosy can broadly be divided into non-specific and specific lesions. In this review, we discuss various oral manifestations in leprosy patients so as to increase the awareness about this aspect among dermatologists and dental surgeons.
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BRIEF REPORT
Piebaldism: A brief report and review of the literature
Saurabh Agarwal, Amit Ojha
May-August 2012, 3(2):144-147
DOI
:10.4103/2229-5178.96722
PMID
:23130293
Piebaldism is a rare autosomal dominant disorder of melanocyte development characterized by a congenital white forelock and multiple symmetrical stable hypopigmented or depigmented macules. We report a family with piebaldism affecting three successive generations and also review the literature.
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CASE REPORTS
Aggressive angiomyxoma of the vulva: An uncommon entity
Mahendra M Kura, Saurabh R Jindal, Usha N Khemani
May-August 2012, 3(2):128-130
DOI
:10.4103/2229-5178.96712
PMID
:23130288
Aggressive angiomyxoma is a rare, locally invasive mesenchymal tumor occurring usually in women of reproductive age, which carries a high risk for local relapse; hence the need to differentiate it from the other mesenchymal tumors occurring in this region. We describe a case of a 44-year-old female presenting with a large pedunculated swelling on the right labia majora.
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ORIGINAL ARTICLES
Comparative study of 15% TCA peel versus 35% glycolic acid peel for the treatment of melasma
Neerja Puri
May-August 2012, 3(2):109-113
DOI
:10.4103/2229-5178.96702
PMID
:23130283
Background:
Chemical peels are the mainstay of a cosmetic practitioner's armamentarium because they can be used to treat some skin disorders and can provide aesthetic benefit.
Objectives:
To compare 15% TCA peel and 35% glycolic acid peel for the treatment of melasma.
Material and Methods:
We selected 30 participants of melasma aged between 20 and 50 years from the dermatology outpatient department and treated equal numbers with 15% TCA and 35% glycolic acid.
Results:
Subjective response as graded by the patient showed good or very good response in 70% participants in the glycolic acid group and 64% in the TCA group.
Conclusions:
There was statistically insignificant difference in the efficacy between the two groups for the treatment of melasma.
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REVIEW ARTICLES
Parthenium the terminator: An update
Chembolli Lakshmi, CR Srinivas
May-August 2012, 3(2):89-100
DOI
:10.4103/2229-5178.96698
PMID
:23130280
Parthenium dermatitis is a distressing dermatitis caused by the air borne allergen of the Compositae weed
Parthenium hysterophorus
. Uncommon presentations, newer insights in pathogenesis and management of this "scourge" are discussed in this article.
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CASE REPORTS
Pigmented epidermal cyst with dense collection of melanin: A rare entity - Report of a case with review of the literature
PS Jayalakshmy, K Subitha, PV Priya, Gerald Johnson
May-August 2012, 3(2):131-134
DOI
:10.4103/2229-5178.96714
PMID
:23130289
Epidermal cyst is a very common benign cystic lesion of the skin. It is usual to find ulceration of the lining epithelium, rupture of the cyst wall with chronic inflammation and foreign body giant cell reaction. But, it is very rare to see an epidermal cyst with marked accumulation of melanin pigment. Only a few cases of pigmented epidermal cyst with dense collection of melanin pigment have been published in the literature. Here, we are reporting a case of ruptured epidermal cyst with keratin granuloma formation and showing dense collection of melanin pigment.
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Mycosis Fungoides: Tumour d'emblee
Rita Vora, Syed Mubashir, Parag Talavia, Gopikrishnan Anjaneyan
May-August 2012, 3(2):122-124
DOI
:10.4103/2229-5178.96709
PMID
:23130286
Mycosis Fungoides is a Cutaneous T-cell lymphoma characterized by infiltration of skin with patches, plaques, and nodules composed of T-lymphocytes. It is the most common type of Cutaneous T-Cell Lymphoma and accounts for almost 50% of all primary cutaneous lymphoma. Tumour d' emblee is the term used for the patient presenting with skin tumors not preceded by patches or plaques. We report a rare case of mycosis fungoides d' emblee variant with tumors of only 3 months duration without any preceding skin lesions.
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3,147
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Hypohidrotic ectodermal dysplasia
Saurabh Agarwal, Shalini Gupta
May-August 2012, 3(2):125-127
DOI
:10.4103/2229-5178.96711
PMID
:23130287
Hypohidrotic ectodermal dysplasia (HED) is a rare genetic disorder characterized by the faulty development of the ectodermal structure, resulting in most notably anhydrosis/hypohydrosis, hypotrichosis and hypodontia. The condition is usually an X-linked recessive disorder affecting predominantly males. We are here reporting a classical case of hypohidrotic ectodermal dysplasia with a review of the literature.
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Dermatitis artefacta
M Kumaresan, Reena Rai, Anju Raj
May-August 2012, 3(2):141-143
DOI
:10.4103/2229-5178.96720
PMID
:23130292
Dermatitis artefacta (DA) is a psychocutaneous disorder where the skin lesions are self self-induced to satisfy an unconscious psychological or emotional need. We report a case of DA where we video recorded the patient self-inducing the lesions.
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GUEST EDITORIAL
On the clinical significance of cutaneous melanoma's precursors
Giuseppe Noto
May-August 2012, 3(2):83-88
DOI
:10.4103/2229-5178.96690
PMID
:23130279
We can identify three main groups of cutaneous pigmented lesions that could be represented as melanoma precursors: (a) congenital melanocytic nevi, (b) dysplastic or atypical nevi, and (c) acquired melanocytic nevi. The occurrence of melanoma in small and intermediate congenital melanocytic nevi is very uncommon, but there is a high risk in large congenital melanocytic nevi, in particular those arising in the so-called "bathing trunk" distribution. It is very important to distinguish the familial dysplastic nevus syndrome, which is a strong risk factor for cutaneous melanoma, from not familial (sporadic) dysplastic nevus, in which the risk for melanoma would depend on the total number of melanocytic nevi, phototype, and on the relationship to environmental factors.
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ORIGINAL ARTICLES
Comorbid conditions in psoriasis - Higher frequency in females: A prospective study
Parimalam Kumar, Jayakar Thomas
May-August 2012, 3(2):105-108
DOI
:10.4103/2229-5178.96701
PMID
:23130282
Aim:
To study the association of obesity, diabetes, hypertension, and abnormal lipid profile in women above 40 years of age with psoriasis.
Materials and Methods:
Two hundred consecutive female patients with psoriasis attending private clinics were included. Complete general, systemic, and dermatological examinations were performed. Blood pressure, blood sugar, and lipid profile were recorded in all patients and the findings analyzed.
Results:
Of 200 patients, 45 were obese. Eighty-eight patients had diabetes mellitus and 29 had dyslipidemia of whom 13 and 18, respectively, were detected at the time of enrolment. All 25 patients with systemic hypertension were on treatment. A total of 177 (88.5%) patients had one or more comorbid conditions. This frequency is much higher when compared to other Indian studies where the sample included patients of both sexes.
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THROUGH THE LENS
Vulval Syringoma: First report of a case in an Egyptian female
Moetaz M El-Domyati, Hamza M Abdel-Raouf, Tarek El-Ammawi, Eman S Abdel-Azim
May-August 2012, 3(2):157-158
DOI
:10.4103/2229-5178.96731
PMID
:23130299
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CASE REPORTS
Disseminated cutaneous cysticercosis and neurocysticercosis: A rare occurrence
S Sacchidanand, P Namitha, M Mallikarjuna, HV Nataraj
May-August 2012, 3(2):135-137
DOI
:10.4103/2229-5178.96716
PMID
:23130290
Disseminated cysticercosis is a parasitic infestation of pork tapeworm,
Taenia solium
. A 19-year-old female presented with multiple nodules all over her body since 12 months. Histopathology showed features suggestive of parasitic granuloma with multinucleated giant cells and plenty of eosinophils admixed with necrosis. Ultrasonography of these lesions showed multiple well-defined cystic lesions of varying size with a few specks of calcification. Cranial computed tomography scan showed bilateral, multiple, small hyperdense lesions in the supratentorial compartment. She was treated with oral albendazole and oral corticosteroids. This case is being reported because of its rare, disseminated nature with cutaneous, neural and ocular involvement.
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LETTERS TO THE EDITOR
Lipoid proteinosis: Histopathological characterization of early papulovesicular lesions
Rameshwar Gutte, Swapnil Sanghvi, Parag Tamhankar, Uday Khopkar
May-August 2012, 3(2):148-149
DOI
:10.4103/2229-5178.96723
PMID
:23130294
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THROUGH THE LENS
Anonychia congenita
Ganesh Avhad, HR Jerajani
May-August 2012, 3(2):156-156
DOI
:10.4103/2229-5178.96729
PMID
:23130298
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CASE REPORTS
Sebaceous carcinoma of scalp with proliferating trichilemmal cyst
Siddhi Chikhalkar, Gaurav Garg, Rameshwar Gutte, Uday Khopkar
May-August 2012, 3(2):138-140
DOI
:10.4103/2229-5178.96718
PMID
:23130291
Sebaceous carcinoma is a rare neoplasm of the sebaceous gland. It is diagnosed mainly on histopathology and, clinically, it may mimic other neoplasms like squamous or basal cell carcinoma. We came across a patient presenting with a non-healing ulcer over the left temporo-parietal region of the scalp since 4 years and a single asymptomatic nodule over the occipital region since 3 years. Histopathology from an ulcer was pathognomonic of sebaceous carcinoma and that from a nodule was suggestive of proliferating trichilemmal cyst. The patient was screened for Muir Torre syndrome. We referred the patient to the oncologist for further management, where the patient was advised complete excision of the lesion.
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LETTERS TO THE EDITOR
Copper chloride antiperspirant action
Ernest Bloom, Howard I Maibach, Jerrold S Polansky
May-August 2012, 3(2):150-151
DOI
:10.4103/2229-5178.96724
PMID
:23130295
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Multiple familial trichoepitheliomas in association with squamous cell carcinoma
Satyaki Ganguly, Kranti C Jaykar, PK Banerjee, Rajesh Kumar, Niyaz Ahmed
May-August 2012, 3(2):151-153
DOI
:10.4103/2229-5178.96726
PMID
:23130296
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SKINDIA QUIZ
SkIndia Quiz 6 - Multiple recurrent erythematous scaly annular plaques in a child
Vidya Kharkar, Viral Thakkar, Rameshwar Gutte
May-August 2012, 3(2):154-155
DOI
:10.4103/2229-5178.93521
PMID
:23130297
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