Home About us Editorial board Ahead of print Current issue Archives Instructions Submit article Search Subscribe Contacts Login
  • Users Online: 113
  • Home
  • Print this page
  • Email this page
Export selected to
Endnote
Reference Manager
Procite
Medlars Format
RefWorks Format
BibTex Format
   Table of Contents - Current issue
Coverpage
January-June 2018
Volume 5 | Issue 1
Page Nos. 1-63

Online since Tuesday, May 29, 2018

Accessed 3,902 times.

PDF access policy
Journal allows immediate open access to content in HTML + PDF
View as eBookView issue as eBook
Author Institution MappingAuthor Institution Mapping
Access StatisticsIssue statistics
RSS FeedRSS
Hide all abstracts  Show selected abstracts  Export selected to  Add to my list
EDITORIAL  

Periorbital hyperpigmentation − An overview of the enigmatous condition Highly accessed article p. 1
Manju Daroach, Muthu S Kumaran
DOI:10.4103/Pigmentinternational.Pigmentinternational_7_18  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
REVIEW ARTICLES Top

Diffuse hyperpigmentation: A comprehensive approach p. 4
Anupama Ghosh, Anupam Das, Rashmi Sarkar
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.
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta

Acral melanosis p. 14
Mala Bhalla, Shimona Garg
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.
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
ORIGINAL ARTICLES Top

A comparative study of psychosocial morbidity in stable versus unstable vitiligo p. 28
Swapna S Khatu, Sharmishtha S Deshpande, Neeta R Gokhale, Deepak Khismtarao, Dipali C Chavan
DOI:10.4103/Pigmentinternational.Pigmentinternational_19_17  
Context: Vitiligo is a cosmetically disfiguring condition especially in dark-skinned individuals, thereby adversely affecting their quality of life (QOL). Studies have reported higher psychiatric morbidity in patients with vitiligo, but a comparative study between patients with stable and unstable vitiligo has not been reported. Aims: To compare the psychiatric morbidity, perceived stress, and QOL in patients suffering from stable versus unstable vitiligo. Settings and Design: This was a clinical observational, cross-sectional liaison study conducted over a period of 2 years and included 100 consecutive patients with vitiligo, who came for treatment to the dermatology clinic of a tertiary care hospital. Materials and Methods: A dermatologist clinically assessed the patients and calculated their vitiligo area severity index score and dermatology life quality index. A psychiatrist evaluated the patients on the basis of the perceived stress scale (PSS), hospital anxiety and depression scale (HADS), and clinically established diagnosis using International Classification of Diseases (ICD-10). Statistical Analysis: The aforementioned variables between the two groups were compared using chi-square test and independent t test. Results: High psychiatric morbidity (65%) was reported in patients with vitiligo, with adjustment disorder being the most common morbidity. The most common reported stress was grief or emotionally significant loss. Psychiatric morbidity, scores on HADS, and PSS were significantly higher in patients with unstable vitiligo in comparison to patients with stable vitiligo. The quality of life (QOL) was mildly affected among the patients in both the groups. Conclusions: There is higher psychiatric morbidity in patients with unstable vitiligo along with a worse QOL in comparison to those with stable vitiligo. Patients with vitiligo should be assessed for stability as well as psychiatric morbidity, because it will have significant management implications.
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta

A study of epidemiological, etiological, and clinicopathological factors in periocular hyperpigmentation p. 34
Manas Chatterjee, Bhabendra Suwal, Ajay Malik, Biju Vasudevan
DOI:10.4103/Pigmentinternational. Pigmentinternational_25_17  
Background: Periocular darkening, popularly known as “dark circles,” is a common condition globally. Pigment deposition, shadowing due to laxity, superficial location of vasculature and prominent nasojugal groove are recognized causative factors. Very few studies exist on its clinicopathological correlation, especially in the Asian population. Materials and Methods: Eighty-two consecutive patients attending skin outpatient department (OPD) with periocular hyperpigmentation (POH) who agreed to follow the study protocol were included in this descriptive study, conducted in Maharashtra, India. They were evaluated clinically and also investigated with histopathology, special staining and immunohistochemistry of the periocular skin to study the various factors involved in the pathogenesis. Results: 19.51% of the patients had a positive family history of POH, 90% gave history of exhaustion of periocular muscles, 41.46% had anemia, 8.54% gave history of aggravation during pregnancy and 7.32% had menstrual irregularities. Laxity of skin was present in 82.92% patients, visible veins in 50%, and sunken eyes with prominent infraorbital rim and shadowing in 26.82%. Periocular darkening due to pigment was present in only 17% patients, with mixed dermoepidermal pigmentation being present in majority (70.73%). Clinicopathological concordance was significant in case of dermal pigmentation (Fisher’s exact test P-value <0.05) in contrast to epidermal. Conclusion: Periocular darkening was predominantly not due to pigment, but rather due to cutaneous laxity and vascular visibility through thin skin. Most of them with pigment had it in the dermis. Clinical dermal pigmentation correlated well with histology, unlike epidermal pigmentation. Iron and amyloid were not significant as etiological factors in our patients.
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
CASE REPORTS Top

Menkes disease: Case report p. 43
Aayushi Mohan, Santhosh K Singh, Anil K Gupta, Amit K Pandey
DOI:10.4103/Pigmentinternational.Pigmentinternational_31_17  
Menkes disease is an X-linked lethal multisystem disorder caused by the disturbances of copper distribution in different tissues due to the mutation of ATPA7 gene. The estimated prevalence of the disease is 1 in 100,000 to 1 in 250,000 (Kirodian et al., 2002).
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta

The appearance of eruptive seborrheic keratoses over linear verrucous epidermal nevus − A report p. 47
Poovanur Sadasivam Subramaniam Ranugha, Jayadev B Betkerur, Tarikere Gangadhar Savitha, Shastry Veeranna, Vijaya Basavaraj
DOI:10.4103/Pigmentinternational. Pigmentinternational_35_17  
Even though seborrheic keratosis (SK)-like histopathological change has been reported within verrucous epidermal nevi (VEN), SKs developing over epidermal nevi has not been described in the past, hence this report. A 50-year-old female presented with asymptomatic pigmented skin lesions over the right half of the body since birth and the appearance of new itchy raised lesions on these of 3 months duration. On examination, multiple verrucous pigmented papules and plaques, along the Blaschko’s lines, were seen involving the right side of the body. Multiple discrete hyperpigmented plaques with a rough surface were seen scattered overlying the linear lesions. There were no similar lesions on the normal skin elsewhere. Investigations for internal malignancy were negative. Biopsy from the linear lesions was suggestive of VEN, while that from the new onset verrucous plaques was consistent with SK. Activating fibroblast growth factor receptor 3 mutations have recently been detected in SKs and VEN. This might explain the colocalization of these in our patient.
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta

Segmental giant café au lait macule in neurofibromatosis 1 p. 50
Bhagyashree B Supekar, Kinjal D Rambhia, Jayesh I Mukhi, Rajesh P Singh
DOI:10.4103/Pigmentinternational. Pigmentinternational_36_17  
A 2-year-old male child born of third degree consanguineous marriage was brought to dermatology outpatient department with multiple dark colored flat lesions over body and one large dark colored flat lesion over right side of body since birth. Another prominent feature was proptosis of left eye since 1 month. Cutaneous examination revealed multiple café au lait macules (CALMs) over lower limbs and back and large CALM over right side of back, chest, and upper limb with proptosis of left eye. Histopathological examination of large patch findings was suggestive of CALM. Magnetic resonance imaging (MRI) brain plain and contrast findings were suggestive of plexiform neurofibroma. Based on clinical features and investigations a diagnosis of giant CALM in segmental distribution in a case of neurofibromatosis 1 (NF1) was made. It can be explained on basis of type II segmental manifestation in NF1.
[ABSTRACT]  [HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
THE CLINICAL PICTURE Top

Maturational hyperpigmentation: Clinico-dermoscopic and histopathological profile of a new cutaneous marker of metabolic syndrome p. 54
Sidharth Sonthalia, Rashmi Sarkar, Shekhar Neema
DOI:10.4103/Pigmentinternational.Pigmentinternational_32_17  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
THROUGH THE DERMOSCOPE Top

Macular amyloidosis in a middle-aged woman p. 57
Piyush Kumar, Shekhar Neema, Niloy Pathak
DOI:10.4103/Pigmentinternational.Pigmentinternational_3_18  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
LETTERS TO THE EDITOR Top

Chikungunya and pigmentation: A tale of two cases p. 59
Shouvik Ghosh, Anupam Das, Piyush Kumar
DOI:10.4103/Pigmentinternational.Pigmentinternational_20_17  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta

Twin Spotting − A Rare Association with Congenital Melanocytic Nevus and Nevus Depigmentosus p. 59
Chitralekha Keisham, Nonita Thokchom, Rashmi Sarkar
DOI:10.4103/Pigmentinternational.Pigmentinternational_21_17  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta

Vitiligo koebnerizing in striae distensae and gravidarum: An interesting clinical phenomenon p. 59
Anuradha Bishnoi, Keshavamurthy Vinay, Muthu S Kumaran, Davinder Parsad
DOI:10.4103/Pigmentinternational. Pigmentinternational_24_17  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
CURRENT BEST EVIDENCE Top

Current best evidence from pigmentary dermatology p. 60
Tanvi Gupta, Rashmi Sarkar
DOI:10.4103/Pigmentinternational.Pigmentinternational_10_18  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta
CROSSWORD Top

PIGMENTCROSS 3 p. 61
Adrija Datta, Zubin Mandlewala, Anupam Das
DOI:10.4103/Pigmentinternational.Pigmentinternational_9_18  
[HTML Full text]  [PDF]  [Mobile Full text]  [EPub]  [Sword Plugin for Repository]Beta

Subscribe this journal
Submit articles
Most popular articles
Joiu us as a reviewer
Email alerts
Recommend this journal