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Armpit rash

Quan Wang, Wen Xia, Deyu Zhao
OBJECTIVE: To analyze the clinical manifestation of interferon gamma receptor 1 deficiency (IFN-γR1 deficiency) and to improve the recognition of this disease in children, decrease diagnostic errors and missed diagnosis. METHOD: The information of one case with IFN-γR1 deficiency (past history of illness, clinical manifestation, laboratory examination and treatment) were analyzed. RESULT: The patient was a 19-month-old girl with IFN-γR1 deficiency, 1-2 weeks after she was vaccinated with BCG at the age of 18 months, she manifested with lymph nodes at the same site as vaccination site, and repeated rash...
May 2014: Zhonghua Er Ke za Zhi. Chinese Journal of Pediatrics
Brijesh Sathian, Sharath Burugina Nagaraja, Indrajit Banerjee, Jayadevan Sreedharan, Asis De, Bedanta Roy, Elayedath Rajesh, Subramanian Senthilkumaran, Syed Ather Hussain, Ritesh George Menezes
BACKGROUND: Breast cancer is the second most common cancer in the world and by far the most frequent cancer among women. OBJECTIVE: The present study was undertaken to assess the awareness of breast cancer warning signs and screening methods among the women of Pokhara valley, Nepal. MATERIALS AND METHODS: A cross-sectional questionnaire survey was carried out in a community setting with the female population. The questionnaire was administered in face-to-face interviews by trained research assistants...
2014: Asian Pacific Journal of Cancer Prevention: APJCP
F Boralevi, M Haftek, P Vabres, S Lepreux, C Goizet, C Leaute-Labreze, A Taieb
BACKGROUND: Hereditary mucoepithelial dysplasia is a dominantly inherited disease, mainly characterized by chronic mucosal lesions associated with keratitis, non-scarring alopecia, keratosis pilaris and perineal intertrigo. Since the original report by Witkop, this condition has been considered to be a disorder of desmosome/gap junction formation, but there has been no ex vivo investigation of these components using genetic and immunolabelling techniques. OBJECTIVES: To perform light and immunoelectron microscopic studies, and partial genetic analysis on five patients in a family and three sporadic cases and to point out similarities of this rare disorder with chronic mucocutaneous candidiasis and other follicular keratosis syndromes, i...
August 2005: British Journal of Dermatology
V D El'kin, B M Datskovskiĭ, L S Mitriukovskiĭ
Bullous ulcerative lichen ruber planus (BULRP) in a 58-year-old woman is described. Besides the common symptoms (papular rash, vesicles and ulcers on the soles, detachment of the nail plates, atrophic foci on the hairy part of the head), the patient has developed erosions on the buccal and vaginal mucosa, articular involvement, complete loss of hair in the armpits and on the pubis. Local dibunol liniment has been effective in therapy of the mucosal erosions.
1989: Vestnik Dermatologii i Venerologii
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