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Chauhan N.S.,Dr Rajendra Prasad Government Medical College Campus | Sharma Y.P.,Dr Rajendra Prasad Government Medical College Campus
Journal of Medical Imaging and Radiation Oncology | Year: 2011

Dual thyroid ectopia is a very rare clinical entity, and only 28 cases have been reported previously in the literature. We describe another case in which CT established the diagnosis preoperatively and prevented an unnecessary surgery. © 2011 The Authors. Journal of Medical Imaging and Radiation Oncology.


Chauhan N.S.,Dr Rajendra Prasad Government Medical College Campus | Sharma Y.P.,Dr Rajendra Prasad Government Medical College Campus | Sharma S.,Dr Rajendra Prasad Government Medical College
Japanese Journal of Radiology | Year: 2011

Complete androgen insensitivity syndrome (CAIS) is a rare X-linked disorder characterized by a female body habitus and male genotype. The Müllerian duct derivatives are absent or rudimentary, and the testes are undescended. Microtia is characterized by a malformed auricle; and in some cases it is genetically transmitted with a non-sex-linked inheritance pattern. The presence of CAIS with microtia has not been documented previously, and this is the first case to describe the radiological findings of this rare presentation. © 2011 Japan Radiological Society.


Raina R.,Dr Rajendra Prasad Government Medical College Campus | Mahajan V.,Dr Rajendra Prasad Government Medical College | Sood A.,Dr Rajendra Prasad Government Medical College | Saurabh S.,Dr Rajendra Prasad Government Medical College Campus
Indian Journal of Dermatology | Year: 2016

A 32-year-old male presented to Dermatology outpatient Department with complaints of a single nonhealing ulcer on his right thigh. This lesion was there for the last 1 months. It had begun as a small nodule and increased up to the present size of 3 cm with an oozing and ulcerated surface and thickened everted margins. The systemic investigations were normal which included hemogram, biochemistry, including liver and renal function tests, chest X-ray, ultrasonography of abdomen, computed tomography of the thorax, and abdomen. Skin biopsy revealed multiple rounds to oval spores with surrounding halo intracellularly as well as extracellularly. A diagnosis of deep fungal infection as histoplasmosis was made and confirmed on culture. © 2016 Indian Journal of Dermatology | Published by Wolters Kluwer - Medknow.


PubMed | Dr Rajendra Prasad Government Medical College Campus
Type: Case Reports | Journal: Japanese journal of radiology | Year: 2011

Complete androgen insensitivity syndrome (CAIS) is a rare X-linked disorder characterized by a female body habitus and male genotype. The Mllerian duct derivatives are absent or rudimentary, and the testes are undescended. Microtia is characterized by a malformed auricle; and in some cases it is genetically transmitted with a non-sex-linked inheritance pattern. The presence of CAIS with microtia has not been documented previously, and this is the first case to describe the radiological findings of this rare presentation.

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