http://old.chanrejournals.com/index.php/casereports/issue/feed Internet Journal of Case Reports 2016-08-29T12:21:56+00:00 Editorial Team editor@chanrejournals.com Open Journal Systems <p>The journal publishes interesting case reports, case series, and brief reports on clinical and laboratory findings across all medical disciplines. It welcomes exceptional case reports that encompass topics in general medicine and allied fields including those dealing with diagnostic challenges, novel therapeutic interventions, or unusual clinical presentations.</p> http://old.chanrejournals.com/index.php/casereports/article/view/194 Thrombotic microangiopathy in membranous lupus nephritis 2016-08-29T12:21:55+00:00 Kiran B Mandya Chikkalingaiah kiranbabumc@gmail.com <p style="text-align: justify;">Renal vascular lesions in SLE are grouped into uncomplicated vascular immune deposits, non-inflammatory necrotizing vasculopathy, thrombotic microangiopathy (TMA) and renal vasculitis. Thrombotic microangiopathy (TMA) is a rare finding in patients with SLE and is associated with poor prognosis. Treatment approach for TMA with membranous nephritis is highly challenging. The present case study discusses the case of a young woman with SLE and membranous lupus nephritis, complicated by TMA.</p> 2016-06-07T00:00:00+00:00 Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/195 A case of Darier-Roussy sarcoidosis 2016-08-29T12:21:55+00:00 Deepak CL dr_deepakcl@yahoo.co.in Renuka Panchagnula drrenuka@chanrediagnostic.com Swetha J drswetha.j31@gmail.com Devaraj Kori devarajkori@gmail.com <p style="text-align: justify;">Subcutaneous sarcoidosis, a rare form of cutaneous sarcoidosis, is seen in approximately 4.3-12.1% of patients with systemic sarcoidosis. These lesions are often associated with less severe systemic disease and usually appear at the beginning of the disease. The present study discusses an unusual case of subcutaneous sarcoidosis with interferon-γ release assay (IGRA) positivity. The case report highlights the increased chances of misdiagnosis of Darier-Roussy sarcoidosis as tuberculosis based on positive IGRA, especially in countries with increased prevalence of TB.</p><br /> 2016-06-06T00:00:00+00:00 Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/187 Alveolar soft part sarcoma: A rare cytological impression 2016-08-29T12:21:55+00:00 Kafil Akhtar kafil_akhtar@yahoo.com Afzal Anees aanees@gmail.com <p style="text-align: justify;"><span>Alveolar soft part sarcoma (ASPS), a malignant soft tissue tumor with unknown etiology, predominantly occurs in the head and neck region, mainly the tongue and the orbit. The characteristic histopathological feature includes alveolar or pseudoglandular pattern, with PAS-positive, diastase-resistant intra-cytoplasmic inclusions. Primary therapy is total resection and adjuvant chemoradiation therapy. The present case study describes a rare case of ASPS of the anterior chest wall in a 15-year-old patient, diagnosed on fine-needle aspiration cytology. Total resection of the tumor with chemo-radiotherapy was performed and the follow-up after 2 years showed neither local recurrence nor distant metastases.</span></p> 2016-05-30T00:00:00+00:00 Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/203 En coup de sabre 2016-08-29T12:21:56+00:00 Swetha J drswetha.j31@gmail.com <p style="text-align: justify;"><em>En coup de sabre</em>, a variant of linear scleroderma, presents as an indented, vertical, colorless, line of skin on the forehead. The indentation appears as a sabre cut on the forehead. It may be associated with atrophy of muscles underlying bone and rarely the brain tissue. The present patient was ANA positive with a negative profile. Based on the findings, the disease was diagnosed as linear scleroderma.</p> 2016-08-29T00:00:00+00:00 Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/199 Ballooning of femoral head in juvenile idiopathic arthritis 2016-08-29T12:21:56+00:00 Chandrashekara S chandrashekara_s@yahoo.com Deepak CL dr_deepakcl@yahoo.co.in <p class="Bodytextarial" style="text-align: justify;">A 22-year-old female patient with oligoarticular juvenile idiopathic arthritis (JIA) visited the outpatient department with difficulty in walking, climbing stairs and getting up from sitting position. She had pain in both hip and knee joints. On examination, she had no tenderness in both knee and hip joints. However, she had severe restriction of movements at both hip joints in all direction. The X-ray shows diffuse osteoporosis and overgrowth of femoral head compared to the acetabular cavity leading to restriction of hip movements (Fig. 1).</p> <p> </p><br /><p> </p> 2016-07-28T00:00:00+00:00 Copyright (c)