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EDITORIAL |
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Dermatology in India and Indian dermatology: A Medico-Historical perspective |
p. 235 |
Amiya K Mukhopadhyay DOI:10.4103/2229-5178.185460 PMID:27559495 |
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REVIEW ARTICLE |
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Microneedling: Advances and widening horizons  |
p. 244 |
Aashim Singh, Savita Yadav DOI:10.4103/2229-5178.185468 PMID:27559496Microneedling is a very simple, safe, effective, and minimally invasive therapeutic technique. It was initially introduced for skin rejuvenation, however, now it is being used for a very wide range of indications including acne scar, acne, post-traumatic/burn scar, alopecia, skin rejuvenation, drug delivery, hyperhidrosis, stretch marks, and many more. Moreover, during the last 10 years, many new innovations have been made to the initial instrument, which was used for microneedling. This technique can be combined with other surgical techniques to provide better results. In particular, it is a very safe technique for dark skin types, where risk of postinflammatory pigmentation is very high with other techniques that damage the epidermis. In this review article, we are updating on the different instruments now available for this procedure, and its efficacy when performed alone or in combination with other techniques for various indications. |
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ORIGINAL ARTICLES |
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Quality of life in patients with erythema nodosum leprosum in Kuala Lumpur, Malaysia |
p. 255 |
Felix B Yap, Sze T Kiung, Jeffrey B Yap DOI:10.4103/2229-5178.185495 PMID:27559497Background: There is a paucity of data on quality of life issues in patients with leprosy suffering from erythema nodosum leprosum (ENL). Thus, we aim to study the effect of ENL on quality of life. Materials and Methods: This cross-sectional study was conducted in Hansen's Clinic, Hospital Kuala Lumpur between January 2010 and December 2013 among patients with multibacillary leprosy using the Dermatology Life Quality Index (DLQI). Results: A total of 153 patients participated with 31.4% suffering from ENL. The mean age at presentation was 40.5 ± 16.49 years. The mean DLQI was 7.1 ± 3.72. Patients with ENL were younger (mean age 36.5 vs. 42.4, P = 0.026), had higher mean bacteriologic index (4.3 vs. 3.8, P = 0.004), had physical deformities (47.9% vs. 31.4%, P = 0.049), and had higher mean DLQI score (9.1 vs. 6.2, P < 0.001). All the DLQI domains were higher in patients suffering from ENL except the treatment domain. Symptoms and feeling was the domain with the largest effect followed by daily activities and leisure. Personal relationship had the lowest effect. Conclusion: Quality of life impairment in patients with leprosy in Malaysia is moderate, with larger effect among patients with ENL. The impairment in ENL is comparable to itchy skin conditions such as urticarial and is worse than chronic skin disease such as psoriasis. Thus, it is essential that management of leprosy incorporate quality of life issues. |
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Misuse of topical corticosteroids on the face: A cross-sectional study among dermatology outpatients |
p. 259 |
Abhijeet Kumar Jha, Rajesh Sinha, Smita Prasad DOI:10.4103/2229-5178.185492 PMID:27559498Background: Topical corticosteroids (TC) are being misused widely on the face without a prescription from the dermatologist. Aim: To evaluate the misuse of TC-containing preparations on the face and the adverse effects due to its application. Materials and Methods: A questionnaire-based analysis was done among patients attending the dermatology outpatient department of a tertiary care hospital between March 2014 and March 2015. Patients with various facial dermatoses were asked about their current use of topical preparations and on further followup questioning, those who revealed the use of TCs (25g or more) continuously or intermittently for a minimum duration of four weeks were included in the study and observed for local adverse effects. Results: A total of 410 patients were observed, 306 were females (74.6%) and 104 were males (25.3%). One hundred and seventy-eight patients (43.4%) used topical steroids alone, 124 (30.2%) used creams containing TC, hydroquinone, and tretinoin, 108 (26.3%) used creams containing a combination of TC, antibiotic, and/or antifungal. One hundred and seventy-six patients (42.9%) bought TC or TC containing creams over the counter on their own, without the prescription of a dermatologist, 35 (8.5%) were recommended TC by a beautician (beauty parlors), 82 (20%) by their friends, family members, or neighbors, 75 (18.2%) by a non-dermatologist practitioner, and 42 (10.2%) by a dermatologist. Limitations: The sample size was small. Conclusion: Dispensing of TCs must be regulated in India; they should only be issued against a doctor's prescription. |
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Clinico-microbiological study of dermatophytosis in a tertiary-care hospital in North Karnataka |
p. 264 |
Tonita M Noronha, Raghavendra S Tophakhane, Shobha Nadiger DOI:10.4103/2229-5178.185488 PMID:27559499Context: The dermatophytoses constitute a group of superficial fungal infections of keratinized tissues, namely, the epidermis, hair, and nails. The distribution and frequency of dermatophytosis and their etiologic agents vary according to the geographic region studied, the socio-economic level of the population, the time of study, the climatic variations, the presence of domestic animals, and age. Aims: The present study was undertaken to assess the clinical profile of dermatophytic infections and to identify the causative fungal species in the various clinical presentations. Settings and Design: This was a hospital-based observational study. Materials and Methods: One hundred and fifty clinically suspected cases of dermatophytosis attending the outpatient department of a tertiary care hospital were included in the study. History was taken, general physical and cutaneous examination was done and details of skin lesions noted. Direct microscopy in 10% KOH (40% KOH for nail) and fungal culture on SDA with 0.05% chloramphenicol and 0.5% cycloheximide was done in every case. Statistical Analysis Used: Statistical analysis was done using SPSS 17.0 software. Chi-square test and contingency coefficient test were used as significant tests for analysis. Results: Out of 150 patients studied, majority belonged to the age group of 21–30 years (22.7%). Male-to-female ratio was 1.63:1. Tinea corporis (24.7%) was the most common clinical type observed. The overall positivity by culture was 40% and by direct microscopy was 59.3%. Trichophyton mentagrophytes was the predominant species isolated (48.3%). Conclusions: The present study reveals the changing trend in the prevalence of dermatophyte species in this part of Karnataka. |
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CASE REPORTS |
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Cystic acantholytic dyskeratosis of the vulva: An unusual presentation of a follicular adnexal neoplasm |
p. 272 |
Kara Melissa Tiangco Torres, Jacqueline M Junkins-Hopkins DOI:10.4103/2229-5178.185482 PMID:27559500Acantholytic dyskeratosis (AD) is a histologic pattern seen in Darier's disease or dyskeratosis follicularis, warty dyskeratoma, and transient AD. This pattern is characterized by suprabasilar clefting, acantholysis, and formation of corps ronds and grains. We present a case of AD that is unique based on its genital location and cystic architecture. A 53-year-old woman presented with an otherwise asymptomatic cyst on her left vulva of uncertain duration. On microscopic examination, there were fragments of cystic epithelium with areas of hypergranulosis, acantholysis, corps ronds, and corps grains formation. These features are felt by the authors to be a unique presentation of a follicular adnexal neoplasm. |
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Dyskeratosis congenita presenting with dysphagia |
p. 275 |
Kalpana Gupta, Swati Tripathi, Nidheesh Agarwal, Anurag Bareth DOI:10.4103/2229-5178.185461 PMID:27559501Dyskeratosiscongenita (DKC) is a genetically heterogeneous disease of defective telomere maintenance that may demonstrate different patterns of inheritance. It is characterized by thetriad of dystrophy of the nails, leukokeratosis of the oral mucosa, and extensive net-like pigmentation of the skin. We report a case ofDKC who presented with a chief complaint of dysphagia. |
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Pachyonychia congenita with late onset (PC tarda) |
p. 278 |
A Sravanthi, P Srivalli, K. V. T. Gopal, T Narayana Rao DOI:10.4103/2229-5178.185463 PMID:27559502Pachyonychia congenita is a rare type of ectodermal dysplasia further classified into 4 types. Cutaneous manifestations seen in most of the cases of Pachyonychia congenita include palmoplantar keratoderma, follicular hyperkeratosis, wedge shaped nails, oral leukokeratosis and woolly hair. A 25-year-old male presented to us with thickened nails and scanty scalp hair. On examination, we noticed hyperkeratotic plaques over both the soles, palmoplantar hyperhidrosis and yellowish discoloration, wedging with subungual hyperkeratosis of all the nails. Follicular hyperkeratotic papules and steatocystoma multiplex were also observed over the scalp and face. The patient had history of natal teeth and on dental examination, lower central incisors were absent. All cutaneous changes in our case had manifested first in the 2nd decade except for natal teeth. All the above features suggested the diagnosis of pachyonychia congenita with late onset (PC tarda), which is an infrequently reported rare variant. |
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Cutaneous metastases from signet cell carcinoma of the gut: A report of two cases |
p. 281 |
Anu Anna George, Dincy Peter, Deepti Masih, Meera Thomas, Susanne Pulimood DOI:10.4103/2229-5178.185462 PMID:27559503Cutaneous metastasis from visceral tumors is a rare entity with a reported incidence between 0.3% and 9.8%. These usually occur late in the course of the disease; the average time interval between the diagnosis of malignancy and presentation of cutaneous metastases has been reported to be 33 months. In rare instances (in about 0.8%–1.3% of patients), cutaneous metastases may be a pointer to an underlying undiagnosed malignancy. We report two patients presenting to us with soft, nodular, cutaneous lesions, which was the manifestation of metastatic signet cell carcinoma arising from the gut. We report these cases owing to their rarity. |
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Fibroepithelioma of Pinkus in continuity with nodular basal cell carcinoma: A rare presentation |
p. 285 |
Atul M Dongre, Uday S Khopkar, Yogesh N Kalyanpad, Prachi V Gole DOI:10.4103/2229-5178.185477 PMID:27559504Fibroepithelioma of Pinkus and nodular basal cell carcinoma (BCC) are different morphological variants of BCC. It is very rare to see both the variants together in a single lesion. Here we report a case of a 56-year-old female who presented with a nodule on the trunk, which on biopsy showed features of both nodular BCC and fibroepithelioma of Pinkus. |
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Huriez syndrome with superadded dermatophyte infection |
p. 288 |
Trupti Surana, Bela Padhiar, Umesh Karia, Purna Pandya DOI:10.4103/2229-5178.185466 PMID:27559505Palmoplantarkeratodermas (PPKs) are a heterogeneous group of hereditary and acquired disorders with underlying gene defects, and characterized by hyperkeratosis of palms and soles with or without other ectodermal and systemic abnormalities. Huriez syndrome is a rare autosomal dominant transgradient type of PPK with high frequency of squamous cell carcinoma in the affected skin. We hereby describe a case of a very rare autosomal dominant PPK in a 40-year-old male patient presenting since birth with PPK extending onto the dorsal aspects of hands and feet with peeling of the skin. The complaints were associated with sclerodactyly, hyperhidrosis, and nail abnormalities. Also superadded dermatophyte infection was observed involving abdomen. No history of loss of any digit. No mucosal, dental, or any systemic involvement was present. No sign of malignancy was noted. Baseline investigations, including ultrasonography of abdomen were normal. Histological findings were nonspecific with only orthohyperkeratosis and acanthosis. Diagnosis was mainly done on clinical grounds. The patient is better with oral retinoids and topical emollients and keratolytics along with antifungal treatment for dermatophyte infection. He is under follow up. |
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Clinical and dermatoscopic features of porokeratosis palmaris et plantaris |
p. 290 |
Satish Udare, Karishma Hemmady DOI:10.4103/2229-5178.185483 PMID:27559506A dermatoscope is an important tool in a dermatologist's armamentarium as it can eliminate the need for a biopsy in a wide array of conditions. Porokeratosis was described by Mibelli and Respighi in 1893, as a disorder of keratinization which on the basis of distribution patterns was described as five clinical variants that portrayed a coronoid lamella on histopathology. We describe a case of asymptomatic, long-standing palmar and plantar pits, which on dermatoscopy showed features suggestive of porokeratosis, which was later reconfirmed by histopathologic sections. This report depicts diagnostic features of porokeratosis and obviates the need for invasive procedures for its diagnosis. |
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Macrodystrophia lipomatosa: Review of clinico-radio-histopathological features |
p. 293 |
Banashree Majumdar, Atul Jain, Debashis Sen, Sanchaita Bala, Pranshu Mishra, Sumit Sen, Projna Biswyas, Akhilesh Behra DOI:10.4103/2229-5178.185465 PMID:27559507We report clinical, radiological, and pathological features of three cases of macrodystrophia lipomatosa, which is characterized by progressive proliferation of all mesenchymal elements, with a disproportionate increase in fibroadipose tissue. The peculiarity in our report is the involvement of contralateral hand and feet in our 1st case in contrast to usual presentations of this rare condition, which is often unilateral. In our 2nd case, the lateral aspect of foot was involved as against the usual finding of involvement of medial aspect in lower limbs, also another surprising finding in this case is increase in the size of lesion after puberty. Coming to our 3rd case, enlargement of almost whole of an upper extremity with profound involvement of middle, ring and little finger along with total sparing of the thumb is in itself an extremely rare occurrence as in upper limb, mainly the lateral aspect of hand and related digits bear the burnt and more over involvement of whole limb is itself an unique phenomenon. |
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Cutaneous tuberculosis with a difference: Documenting transfollicular elimination of granulomas |
p. 297 |
Chirag A Desai, Uday Khopkar DOI:10.4103/2229-5178.185473 PMID:27559508A patient presented with a an asymptomatic brown to erythematous, scaly indurated solitary plaque on his elbow. The lesion was diagnosed as lupus vulgaris on the basis of clinical features and biopsy findings. The histopathology further revealed a granuloma within the follicular infundibulum, which was possibly being expelled out. The phenomenon of transepidermal elimination has been described previously in many conditions, including cutaneous tuberculosis; however, transfollicular elimination of the granuloma has not been reported. We report this unusual phenomenon as a possible mode of elimination of the granuloma. |
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Erythema elevatum diutinum in association with IgA monoclonal gammopathy: A rare case report |
p. 300 |
Guru Prasad Patnala, Anila P Sunandini, Rama Rayavarapu, Padmasri Somala Yandapalli DOI:10.4103/2229-5178.185472 PMID:27559509Erythema elevatum diutinum (EED) is a rare form of vasculitis characterized clinically by red-violet brown papules, plaques, and nodules mainly involving the extensor surfaces; histologically by leukocytoclastic vasculitis in early lesions, and fibrosis and cholesterolosis in late lesions. EED has been associated with many systemic disorders including infections, autoimmune disorders, and both benign and malignant hematological disorders. As it is a rare form of vasculitis and only 250 cases reported till date, we report a case of EED in association with IgA monoclonal gammopathy with partial response to dapsone treatment. |
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Seronegative necrolytic acral erythema: A report of two cases and literature review |
p. 304 |
Vishalakshi S Pandit, Arun C Inamadar, Aparna Palit DOI:10.4103/2229-5178.185464 PMID:27559510Necrolytic acral erythema (NAE) is a newly described entity, seen in patients infected with hepatitis C virus. It is characterized by its distinguishing acral distribution, psoriasiform skin eruption and histological features. Its etiopathogenesis is not fully understood though hypo amino academia, hyperglucagonemia and zinc deficiency are considered as probable causes. In 1996, El Darouti and Abu el Ela first described this entity in seven Egyptian patients with hepatitis C virus (HCV). Since then, several small studies and cases have been reported around the world. Nevertheless, it may occur independently without HCV association as a few cases have been reported recently. We report two seronegative cases of NAE, which responded dramatically with oral zinc therapy. This suggests that NAE could be an isolated clinical subset. |
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CASES FROM ACKERMAN ACADEMY |
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Cellular dermatofibroma: A hyperkeratotic indurated plaque on the thigh |
p. 308 |
Amira Elbendary, John R Griffin, Dirk M Elston, Shyam B Verma DOI:10.4103/2229-5178.185497 PMID:27559511 |
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DRUG PROFILE |
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Vitamin E in dermatology  |
p. 311 |
Mohammad Abid Keen, Iffat Hassan DOI:10.4103/2229-5178.185494 PMID:27559512Vitamin E is an important fat-soluble antioxidant and has been in use for more than 50 years in dermatology. It is an important ingredient in many cosmetic products. It protects the skin from various deleterious effects due to solar radiation by acting as a free-radical scavenger. Experimental studies suggest that vitamin E has antitumorigenic and photoprotective properties. There is a paucity of controlled clinical studies providing a rationale for well-defined dosages and clinical indications of vitamin E usage in dermatological practice. The aim of this article is to review the cosmetic as well as clinical implications of vitamin E in dermatology. |
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LETTERS TO THE EDITOR |
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Idiopathic hemihypertrophy with multiple fibroadenoma |
p. 316 |
Asha Nyati, Sarita Kalwaniya, Parul Agarwal DOI:10.4103/2229-5178.185481 PMID:27559513 |
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Lupus vulgaris in classical sporotrichoid pattern |
p. 317 |
Manjulata Dash, Swetalina Pradhan DOI:10.4103/2229-5178.185491 PMID:27559514 |
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Necrotizing fasciitis associated with systemic lupus erythematosus in a child |
p. 319 |
Sahana M Srinivas, Alkarani T Patil, Gowri Shankar, Keshavmurthy M Lakshmikantha, Munirathnam Govindraj DOI:10.4103/2229-5178.185498 PMID:27559515 |
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COMMENTARY |
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Necrotizing fasciitis associated with systemic lupus erythematosus in a child |
p. 319 |
Mahmood Dhahir Al-Mendalawi DOI:10.4103/2229-5178.185496 PMID:27626093 |
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LETTERS TO THE EDITOR |
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A rare case of multiple keratoacanthomas treated with oral acitretin and intralesional methotrexate |
p. 321 |
Sweta Hasmukh Rambhia, Kinjal Deepak Rambhia, Amit Gulati DOI:10.4103/2229-5178.185480 PMID:27559516 |
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Eyelid excoriation and erythema with nepafenac eye drop |
p. 324 |
Kumar Saurabh, Rupak Roy, Debmalya Das, Aneesha Lobo DOI:10.4103/2229-5178.185478 PMID:27559517 |
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Reactive eccrine syringofibroadenoma in hyperkeratotic eczema |
p. 325 |
Chirag A Desai, Uday Khopkar DOI:10.4103/2229-5178.185476 PMID:27559518 |
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Aquagenic syringeal acrokeratoderma |
p. 327 |
Amit Kumar Dhawan, Kavita Bisherwal, Vijay Gandhi, Prachi Kawthekar, Preeti Diwaker DOI:10.4103/2229-5178.185490 PMID:27559519 |
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Giant bilateral Becker's nevus appearing as gladiator arm armor |
p. 329 |
Premanshu Bhushan, Sarvesh S Thatte DOI:10.4103/2229-5178.185469 PMID:27559520 |
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Half and half blisters in pemphigus vulgaris: A diagnostic quandary |
p. 331 |
Shagufta Rather, Atiya Yaseen, Iffat Hassan DOI:10.4103/2229-5178.185487 PMID:27559521 |
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Pyoderma gangrenosum associated with mantle cell lymphoma |
p. 332 |
Tanmay Padhi, Swetalina Pradhan, Krupasindhu Pradhan, Suresh K Kumar DOI:10.4103/2229-5178.185467 PMID:27559522 |
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Comparative assessment of the efficacy of topical ketoconazole and topical luliconazole in cases of pityriasis versicolor at a tertiary care hospital in eastern India: A prospective, open, randomized controlled trial  |
p. 335 |
Somenath Sarkar, Dipayan Sengupta, Sukumar Basak, Shabab Ahmed Damji, Devesh Kumar Shukla, Deep Anurag DOI:10.4103/2229-5178.185471 PMID:27559523 |
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Cerebrotendinous xanthomatosis |
p. 336 |
Mahalakshmi Muniaswamy, Madhu Rengasamy, Ramesh Aravamuthan, Manoharan Krishnasamy DOI:10.4103/2229-5178.185484 PMID:27559524 |
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Acral lentiginous melanoma with multiple brain metastases in an Indian male |
p. 338 |
Kumar Parimalam, Jeyalakshmidevi Namasivayam, Subha Ramasamy, Suganthy Valavan DOI:10.4103/2229-5178.185474 PMID:27559525 |
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Annular atrophic plaque over the arm |
p. 340 |
Amit Kumar Dhawan, Kavita Bisherwal, Chander Grover, Preeti Diwaker DOI:10.4103/2229-5178.185486 PMID:27559526 |
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A study of postherpetic pruritus |
p. 343 |
Asit Mittal, Ankita Srivastava, Manisha Balai, Ashok Kumar Khare DOI:10.4103/2229-5178.185479 PMID:27559527 |
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Extrafacial melasma over forearms |
p. 344 |
Bhushan Madke, Sumit Kar, Nidhi Yadav, Pooja Bonde DOI:10.4103/2229-5178.185470 PMID:27559528 |
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Trigeminal trophic syndrome |
p. 346 |
Lalit Kumar Gupta, Ankita Srivastava, Ashok Kumar Khare, Asit Mittal, Sharad Mehta, Manisha Balai DOI:10.4103/2229-5178.185485 PMID:27559529 |
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SKINDIA QUIZ |
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Sk India Quiz 26: Hypopigmented papules in a human immunodeficiency virus-positive patient |
p. 348 |
Lalit Kumar Gupta, Manisha Balai, Ashok Kumar Khare, Asit Mittal DOI:10.4103/2229-5178.182402 PMID:27559530 |
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SkIndia Quiz 27: Rhinophyma and numerous facial papule and nodules in a 39-year-old woman |
p. 350 |
Vikram K Mahajan, Anju Lath Sharma, Pushpinder S Chauhan, Karaninder S Mehta, Saurabh Sharma DOI:10.4103/2229-5178.182404 PMID:27559531 |
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THROUGH THE LENS |
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Mycetoma |
p. 353 |
Angoori Gnaneshwar Rao DOI:10.4103/2229-5178.185489 PMID:27559532 |
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Black discoloration of palms |
p. 356 |
Feroze Kaliyadan, KT Ashique DOI:10.4103/2229-5178.185493 PMID:27559533 |
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OBITUARY |
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Dr. Balbir S. Bhogal (1950–2016) |
p. 357 |
Amrinder J Kanwar DOI:10.4103/2229-5178.185475 |
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