Home About us Editorial board Ahead of print Current issue Archives Instructions Submit article Search Subscribe Contacts Login
  • Users Online: 671
  • Home
  • Print this page
  • Email this page
Export selected to
Endnote
Reference Manager
Procite
Medlars Format
RefWorks Format
BibTex Format
  Most popular articles (Since April 10, 2014)

 
 
  Archives   Most popular articles   Most cited articles
 
Hide all abstracts  Show selected abstracts  Export selected to
  Viewed PDF Cited
REVIEW ARTICLE
Lichen planus pigmentosus: A short review
Irene Mathews, Devinder Mohan Thappa, Nidhi Singh, Debasis Gochhait
January-June 2016, 3(1):5-10
DOI:10.4103/2349-5847.184265  
Lichen planus pigmentosus (LPP) is a condition characterized by persistent and asymptomatic slaty-gray pigmentation, predominantly in the face. Classically, the pattern is “actinic” with symmetric and diffuse pigmentation in sun-exposed areas, commonly in dark-skinned individuals. It can also rarely present as macular pigmentation of the flexures in the lighter-skinned. LPP is a disease of the middle-aged, with onset in the third to fourth decades of life and few studies show as slightly greater incidence in females. The photo-distributed or actinic pattern, which is more common, is a disease of tropics and Type IV–Type V skin types. Reports are mainly from India, the Middle East, and South America. The inversus type is relatively rare, predominantly occurring in Caucasians. LPP is thought to be a type hypersensitivity IV reaction to unknown antigen with lichenoid inflammation, leading to melanin incontinence and superficial dermal pigmentation. The natural course of the disease is not clear with some cases showing spontaneous resolution, and some cases with persistence of pigmentation for years. In addition, LPP may have marked overlap clinically and histologically with conditions such as pigmented contact dermatitis, differentiation of which may not be possible in routine practice. Because of these issues, as well as the relative rarity of the condition, there is not much evidence on the efficacy of the various treatment options. Currently, none of the available treatment options show consistent responses or a clear superiority to other modalities, the evidence on efficacy being restricted to a few case series.
  35,924 1,683 3
REVIEW ARTICLES
Pigmentary demarcation lines
Nidhi Singh, Devinder Mohan Thappa
January-June 2014, 1(1):13-16
DOI:10.4103/2349-5847.135431  
Pigmentary demarcation lines (PDLs) are areas of an abrupt transition from hyperpigmented to hypopigmented or normal skin color. They are seen on limbs, face, and sometimes trunk. They are common in the black race. There are eight groups of PDL A to H. Facial PDL should be differentiated from melasma and postinflammatory pigmentation over the face. PDL are common in black women during pregnancy and are considered to be normal variants of pigmentation. Etiology of PDL continues to be an enigma and needs further research. PDL in pregnancy may regress spontaneously after delivery and do not require treatment. Facial PDL have a persistent course posing cosmetic concern for the patient and a challenge for dermatologist.
  19,509 1,049 1
A brief review of nevus depigmentosus
Samujjala Deb, Rashmi Sarkar, Asit Baran Samanta
July-December 2014, 1(2):56-58
DOI:10.4103/2349-5847.147041  
Nevus depigmentosus is a congenital disorder of pigmentation which occurs in all sexes and races. It commonly presents in childhood and is mostly nonprogressive. It is a form of cutaneous mosaicism with functionally defective melanocytes and abnormal melanosomes. Localized solitary lesions need to be differentiated from conditions like nevus anemicus, ash leaf macule, vitiligo, etc., and generalized lesions from hypomelanosis of Ito. Treatment is usually not required although cosmetic camouflage, phototherapy, grafting, and other modalities may be tried.
  17,397 809 1
Recent advances in melasma
Manas Chatterjee, Biju Vasudevan
July-December 2014, 1(2):70-80
DOI:10.4103/2349-5847.147044  
Melasma is one of the most common pigmentary disorders worldwide with a still unresolved pathogenesis and treatment continues to be challenging. Increased sun exposure and genetic factors are considered the two most important etiological factors. Estrogens, progesterones and increased melanocyte stimulating hormone are also involved. Melasma treatment can be very frustrating as many modalities can turn out to be ineffective. Dermal and mixed variants are quite resistant to therapy. Most patients seek medical help much after the onset of the condition, making treatment even more difficult. Sunscreens and topical depigmenting agents remain mainstay of therapy. Chemical peels and light sources are beneficial as adjuncts. There have been numerous advances in the understanding and management of melasma. This review attempts to look at these newer vistas in melasma. Literature search for the review was done from PubMed, the Cochrane Library, MEDLINE and Embase using the key word "melisma," "melasma pathogenesis" and "melasma treatment."
  13,510 1,491 -
REVIEW ARTICLE
Tranexamic acid: An emerging depigmenting agent
Anju George
July-December 2016, 3(2):66-71
DOI:10.4103/2349-5847.196295  
Tranexamic acid (TXA), an antifibrinolytic drug, is now gaining popularity as a depigmenting agent. It is a synthetic lysine amino acid derivative which mainly blocks the conversion of plasminogen to plasmin by inhibiting plasminogen activator. This results in less free arachidonic acid production, and hence a reduction in the prostaglandin (PG) levels as well. Thus, by reducing PG production, TXA reduces the melanocyte tyrosinase activity and plays an important role in the treatment of melasma, ultraviolet-induced hyperpigmentation, and other postinflammatory hyperpigmentation. It has been tried topically, orally, and intradermally in the management of melasma with minimal adverse effects. However, more randomized trials are needed to fully elucidate the exact mechanism of action, ideal route, frequency, and duration of administration of the drug, along with its potential to treat other pigmentary disorders.
  13,245 1,247 -
REVIEW ARTICLES
Acral melanosis
Mala Bhalla, Shimona Garg
January-June 2018, 5(1):14-27
DOI:10.4103/Pigmentinternational.Pigmentinternational_15_17  
The term “acral” means the distal portions of the limbs (hand, foot) and the head (ears, nose). The term acral melanosis is loosely applied to an increase in melanin pigmentation, in a diffuse, reticulate, or focal pattern over the distal parts of the arms and legs. There are various causes of acral pigmentation varying from genetic to acquired, benign to malignant, autoimmune to infectious, drug-induced, nutritional deficiencies, postinflammatory, and even exogenous reasons. The pigmentation may be occurring in isolation or associated with various systemic features. An earlier age of the onset of pigmentation, a positive family history, and a reticulate or mottled pattern usually point to a genetic cause. The diffuse pattern of pigmentation is usually seen in racial, endocrine diseases, and nutritional deficiencies. Postinflammatory acral pigmentation may follow both infectious and autoimmune diseases and may even be drug induced. A correct diagnosis is important to decide on the management which varies from reassurance and counseling to active treatment. This review paper is an attempt to classify acral pigmentation based on its diverse etiological causes.
  13,888 562 -
CASE REPORTS
Linear lichen planus pigmentosus: A rare entity with an illusory presentation
Anupam Das, Vivek Mishra, Indrashis Podder, Piyush Kumar, Dipti Das, Nilay Kanti Das
July-December 2014, 1(2):100-102
DOI:10.4103/2349-5847.147048  
We report a case of lichen planus pigmentosus (LPP) that developed in a linear pattern, that too over nonsun-exposed areas. The patient presented with linear dark brown macules and patches on the back in the midline. Skin biopsy showed features consistent with a diagnosis of LPP. LPP should be considered in the clinical differentials of linear hyperpigmented skin lesions.
  12,638 433 2
REVIEW ARTICLES
Stem cells in vitiligo: Current position and prospects
Keshavamurthy Vinay, Sunil Dogra
January-June 2014, 1(1):8-12
DOI:10.4103/2349-5847.135430  
Skin is an easily accessible source of various sub population of stem cells including epidermal stem cells, hair follicle stem cells (HFSCs) and dermal mesenchymal stem cells. The outer root sheath (ORS) of the hair follicle is a rich source of a type of HFSCs called the melanocytes stem cells (MelSCs). These HFSCs have a vast, unexplored potential in the treatment of vitiligo as initial re-pigmentation often occurs around the hair follicles. Common therapeutic modalities such as tacrolimus, phototherapy and dermabrasion acts through MelSCs. Newer cellular techniques have explored the use of ORS hair follicle suspension in surgical treatment of vitiligo. Advancement in melanocyte and stem cell research has identified various cytokines, growth factors and regulators involved in proliferation and differentiation of melanoblasts, which can be used for autologous in situ melanocyte regeneration. In this review, we briefly discuss the current position and future prospects of stem cells in vitiligo.
  11,549 1,141 4
Postinflammatory hyperpigmentation: Review of pathogenesis, prevention, and treatment
Anisha B Patel
July-December 2014, 1(2):59-69
DOI:10.4103/2349-5847.147043  
Postinflammatory hyperpigmentation (PIH) is a common pigmentary disorder that is distressing to patients, particularly those with skin of color, and can be very difficult to treat. Part of this difficulty arises from the dermal melanosis in addition to the epidermal hyperpigmentation. This article reviews the mechanisms that induce the hyperpigmentation including inflammatory mediators such as metabolites of arachidonic acid and reactive oxygen species (ROS) and how these may influence prevention and treatment strategies. Treating the inflammatory cause and sun protecting are crucial to effective therapy. Although common, few studies have been done focusing on prevention and treatment of this disease. Topical therapies are the mainstay of treatment for PIH, but have shown poor efficacy for the dermal hyperpigmentation component. Hydroquinone in combination with topical steroids, retinoids, glycolic acid, and lactic acid have been augmented with numerous emerging natural therapies such as kojic acid, arbutin, ascorbic acid, soy, and niacinamide. Although efficacious for hyperpigmentation, most of the natural therapies have not been studied specifically for PIH. Salicylic acid and glycolic acid chemical peels, as well as the quality-switched (QS) neodymium-doped yttrium aluminum garnet (Nd: YAG), QS Ruby, 1550 nm erbium fiber fractional thermolysis, and 1927 nm fractional thulium fiber lasers have shown good efficacy for the treatment of facial hyperpigmentation.
  11,171 1,361 1
Progressive macular hypomelanosis: An update
Seemal R Desai, Joshua L Owen
July-December 2014, 1(2):52-55
DOI:10.4103/2349-5847.147040  
Progressive macular hypomelanosis (PMH) is a common and often misdiagnosed disorder characterized by numerous nummular, coalescing hypopigmented macules on the trunk of adolescents, and young adults. It was originally described in patients with Fitzpatrick skin types V-VI from tropical countries, but is now understood to have a worldwide distribution in a variety of skin types. The pathogenesis of PMH is unknown, but is thought to involve Propionibacterium acnes, which has been found in abundance in the pilosebaceous units of lesional skin. Biopsies of lesions demonstrate normal architecture of epidermis and dermis, but exhibit decreased melanin content. It is important to note that this is different from vitiligo, which has a total absence of melanin. Many patients with PMH often times go misdiagnosed for tinea (pityriasis) versicolor, postinflammatory hypopigmentation, and other dyschromias. Topical antifungal and corticosteroid therapy have proven ineffective in PMH, but successes have been reported with topical and systemic antibacterial treatment modalities and even phototherapy. Given the increasing prevalence of patients with skin of color, it is important to better understand the nature of this condition, along with its diagnosis, management, and treatment.
  11,828 662 1
FOCUS
The enigma of color in tinea versicolor
Divya Gupta, Devinder Mohan Thappa
January-June 2014, 1(1):32-35
DOI:10.4103/2349-5847.135440  
  11,142 724 -
EDITORIALS
Skin pigmentation in relation to gender: truth and myth
Rashmi Sarkar, Shivani Bansal
January-June 2017, 4(1):1-2
DOI:10.4103/2349-5847.208350  
  7,946 302 -
REVIEW ARTICLES
Narrowband ultraviolet B and beyond: Evolving role of phototherapy in vitiligo
Amanjot K Arora, Sunil Dogra
January-June 2015, 2(1):9-20
DOI:10.4103/2349-5847.159387  
Vitiligo is an acquired depigmentation disorder with great impact on patient's appearance and quality of life. Till date, the etiology of vitiligo remains elusive, which makes it difficult to have curative therapies. Photochemotherapy (psoralen and ultraviolet A) long remained the mainstay of treatment of vitiligo, until the advent of narrowband ultraviolet B (NBUVB) phototherapy, which revolutionized the treatment of vitiligo with better results, tolerability and side effect profile than the former. It has been used favorably, both alone as well as in combination with other agents like topical calcineurin inhibitors, Vitamin-D analogs, oral and topical corticosteroids, antioxidants, etc. Recently, various new phototherapeutic modalities like excimer light and laser have come into use with encouraging results. In this article, we review the journey of NBUVB so far and highlight the current status of other new phototherapy modalities in the treatment of vitiligo.
  7,566 616 1
Physiologic pigmentation: Molecular mechanisms and clinical diversity
Cecilia A Larocca, Roopal V Kundu, Neelam A Vashi
July-December 2014, 1(2):44-51
DOI:10.4103/2349-5847.147039  
Dyschromia is one of the leading diagnoses in skin of color of populations. Inclusive within this broad realm of diagnoses includes physiologic pigmentation, which refers to normal biologic variations in skin coloration. In order to properly diagnose and manage disorders of pigmentation, one must be aware of the normal variations in skin pigmentation. Our review summarizes molecular mechanisms and the diverse patterns of physiologic pigmentation that may be encountered in the clinic and that are especially common in richly pigmented individuals.
  5,852 2,130 2
Diffuse hyperpigmentation: A comprehensive approach
Anupama Ghosh, Anupam Das, Rashmi Sarkar
January-June 2018, 5(1):4-13
DOI:10.4103/Pigmentinternational.Pigmentinternational_8_17  
Skin color is determined by melanin and other chromophores and is influenced by physical factors (ultraviolet radiation) and other endocrine, autocrine, and paracrine factors. Being the largest organ of the body, any aberration in skin color (hyperpigmentation and hypopigmentation) can have impact on the patients’ quality of life. Hyperpigmentation may be circumscribed or diffuse. Diffuse hyperpigmentation can be multifactorial in origin; hence, a multipronged approach is needed in such cases. First, the cause (systemic or cutaneous) needs to be ascertained, and then disease-specific management needs to be performed. The biggest challenge in such cases is to treat the hyperpigmentation itself; hence, counseling and general treatment (the use of broad-spectrum sunscreen, the avoidance of sun exposure, etc.) play crucial role, and an interdisciplinary approach may be required, especially when the hyperpigmentation is due to a systemic cause.
  7,039 734 -
EDITORIALS
Glutathione for skin lightning: an update
Sidharth Sonthalia, Rashmi Sarkar
January-June 2017, 4(1):3-6
DOI:10.4103/2349-5847.208348  
  6,603 802 1
EDITORIAL
Role of dermoscopy in the diagnosis of pigmentary dermatoses in skin of color
Sunil Dogra, Ankit Mittal
July-December 2014, 1(2):41-43
DOI:10.4103/2349-5847.147037  
  3,791 3,378 -
CASE REPORTS
Talon noir: A mirage of melanoma
Subramaniam Keerthi, Sankar Madhavi, Kaliaperumal Karthikeyan
January-June 2015, 2(1):54-56
DOI:10.4103/2349-5847.159399  
A 45-year-old female patient presented with two black plaques over her toes for the past 3 months that were persistent without any changes in the color, size or surface. Histopathology showed epidermal hyperplasia with corneal collection of fibrinous proteinaceous material and hemosiderin-laden macrophages and fibrinous exudate. We report this case to highlight the importance of proper diagnosis by means of dermoscopy and paring, of any black patch over acral regions in order to exclude the more concerning acral lentiginous melanoma.
  6,719 224 -
EDITORIAL
Topical therapy in vitiligo: What is new?
Munisamy Malathi, Devinder Mohan Thappa
January-June 2016, 3(1):1-4
DOI:10.4103/2349-5847.184247  
  6,296 628 1
REVIEW ARTICLES
Idiopathic guttate hypomelanosis: An overview
Indrashis Podder, Rashmi Sarkar
July-December 2018, 5(2):83-90
DOI:10.4103/Pigmentinternational.Pigmentinternational_17_18  
Idiopathic guttate hypomelanosis is a commonly acquired, benign leukoderma characterized by multiple, discrete round or oval, porcelain-white macules on sun-exposed areas, especially the extensor aspect of forearms and shins, sparing the face, neck, and trunk. It usually affects the geriatric population (>50 years); chronic exposure to ultraviolet rays and senile degeneration being the important pathogenic factors. The diagnosis remains essentially clinical, whereas newer confirmatory investigations are emerging. Despite the benign course of progression, many patients seek medical attention owing to cosmetic concerns. Several treatment modalities have been tried over time including topical, physical, and surgical measures, although there is lack of a standard treatment regime. In this article, we have reviewed the different aspects of this condition including treatment, along with the recent updates to create awareness about this dermatological entity.
  6,414 340 -
EDITORIAL
Premature graying of hair: The voids and tiffs
Sidharth Sonthalia, Rashmi Sarkar
July-December 2015, 2(2):73-75
DOI:10.4103/2349-5847.172774  
  3,012 3,202 1
REVIEW ARTICLES
Pathogenesis of vitiligo: An update
Amanjot K Arora, Muthu S Kumaran
July-December 2017, 4(2):65-77
DOI:10.4103/2349-5847.219673  
Vitiligo is the most common depigmentary disorder that has been affecting human lives across centuries. Despite its high prevalence, not much can be said precisely about its pathogenesis. Over the years, several theories based on a lot of research have been put forward and many more are coming up each day. This article aims to summarise the various theories put forward so far and highlight the Recent updates in each of them.
  5,366 816 1
SPOT THE DIAGNOSIS
Asymptomatic hypopigmented macules on the trunk and limbs of a young male
Soumya Jagadeesan, Malini Eapen, Jacob Thomas
January-June 2016, 3(1):52-53
DOI:10.4103/2349-5847.184266  
  5,835 199 -
ORIGINAL ARTICLES
A clinico-epidemiological study of facial melanosis
Iffat Hassan, Samia Aleem, Yasmeen Jabeen Bhat, Parvaiz Anwar
January-June 2015, 2(1):34-40
DOI:10.4103/2349-5847.159394  
Background: Facial melanosis is a group of heterogenous entities, sharing a common clinical feature of altered pigmentation of the face and thus easily visible cosmetic disfigurement and significant psychosocial consequences. The importance of these disorders is growing, as they form the major percentage of dermatology consultations. Aims: To assess the patients of facial pigmentary disorders for demographic, etiological and clinical profile. Methods: This prospective hospital-based clinical study, conducted in a tertiary center over 1-year, involved 208 patients with facial pigmentary disorders, assessed using detailed history taking and clinical examination for demographic, etiological and clinical data. Relevant investigations including the skin biopsy and patch testing were also done wherever required. Results: The maximum number of patients belonged to 21-40 years age group (56.73%). Females predominated the study, with a female to male ratio of 1.92: 1. Among patients of facial hypermelanosis, melasma was the most common comprising of 73 patients, followed by postinflammatory hyperpigmentation (35), periorbital hyperpigmentation (14), ephelides (10) and lichen planus pigmentosus (9). Riehl's melanosis (8), drug-induced hyperpigmentation (6), naevoid hyperpigmentation (1), acanthosis nigricans (1) and Addison's disease (1) were other hypermelanosis conditions. Pityriasis alba (22) was the most common cause of facial hypomelanosis followed by vitiligo (19), postinflammatory hypopigmentation (8) and leprosy (1). Almost all cases of facial hyperpigmentation gave history of exacerbation following sun exposure. Conclusion: A variety of pigmentary disorders, both hyper and hypopigmentation, with variable clinical presentations and etiological factors, and associated with significant distress affect the face.
  5,407 570 -
EDITORIALS
Skin color matters in India
Devinder Mohan Thappa, Munisamy Malathi
January-June 2014, 1(1):2-4
DOI:10.4103/2349-5847.135419  
  5,354 506 -