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Background: Cutaneous leishmaniasis in India is mainly confined to the deserts of Rajasthan; some cases have been reported from the dry north-western half of the Indo-Gangetic plain, including Punjab, Himachal Pradesh, Delhi and Varanasi.Aims: To highlight a new focus of cutaneous leishmaniasis in the Jammu division of Jammu and Kashmir State, previously a non-endemic area. This report presents the clinico-epidemiological and investigative results of 120 new cases of cutaneous leishmaniasis detected between November 2012 and October 2013.Methods: The clinical diagnosis of cutaneous leishmaniasis was made using criteria proposed by Bari and Rahman. It was further confirmed by the demonstration of Leishman-Donovan bodies in Leishman stained slit skin smears and skin biopsy specimens, and/or by a satisfactory response to intra-lesional sodium stibogluconate given weekly for 4 weeks. Serial clinical photographs were taken before giving injections and at the end of the 6 th week.Results: There were 67 females and 53 males with an age range of 8 months to 80 years. The most frequently affected site was the face. Lesions were most commonly of the nodulo-ulcerative type. The number of lesions ranged from 1 to 4. Farmers (28.1%), homemakers (27.2%) and students (27.2%) were significantly over-represented among the occupations (P < 0.001). Skin smears and biopsies were positive for Leishman-Donovan bodies in 50.8% and 44.2% cases, respectively.Conclusions: There is a new focus of cutaneous leishmaniasis in Jammu division which deserves urgent attention from the public health angle. Further epidemiological studies are warranted to establish the identity of the vector and the strain of Leishmania involved. [ABSTRACT FROM AUTHOR]

A letter to the editor is presented on the effectiveness of pentoxifylline and sulfasalazine for treatment of pemphigus. [ABSTRACT FROM AUTHOR]

The article focuses on the impact of the cutaneous changes appeared during pregnancy. It states that the said changes cause for substantial anxiety on the part of the prospective mother. It mentions that the changes are due to de novo production of a variety of protein and steroid hormones by the fetoplacental unit as well as the increased activity of maternal pituitary, thyroid and adrenal glands.

A letter to the editor is presented which discusses Kindler's syndrome, a rare genetic disorder characterized by poikiloderma congenitale and epidermolysis bullosa.