Internet Journal of Case Reports http://old.chanrejournals.com/index.php/casereports <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> en-US editor@chanrejournals.com (Editorial Team) techteam@chanrejournals.com (Technical team,IJCR) Mon, 30 May 2016 12:23:25 +0000 OJS 3.3.0.11 http://blogs.law.harvard.edu/tech/rss 60 Thrombotic microangiopathy in membranous lupus nephritis http://old.chanrejournals.com/index.php/casereports/article/view/194 <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> Kiran B Mandya Chikkalingaiah Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/194 Tue, 07 Jun 2016 00:00:00 +0000 A case of Darier-Roussy sarcoidosis http://old.chanrejournals.com/index.php/casereports/article/view/195 <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 /> Deepak CL, Renuka Panchagnula, Swetha J, Devaraj Kori Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/195 Mon, 06 Jun 2016 00:00:00 +0000 Alveolar soft part sarcoma: A rare cytological impression http://old.chanrejournals.com/index.php/casereports/article/view/187 <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> Kafil Akhtar, Afzal Anees Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/187 Mon, 30 May 2016 00:00:00 +0000 En coup de sabre http://old.chanrejournals.com/index.php/casereports/article/view/203 <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> Swetha J Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/203 Mon, 29 Aug 2016 00:00:00 +0000 Ballooning of femoral head in juvenile idiopathic arthritis http://old.chanrejournals.com/index.php/casereports/article/view/199 <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> Chandrashekara S, Deepak CL Copyright (c) http://old.chanrejournals.com/index.php/casereports/article/view/199 Thu, 28 Jul 2016 00:00:00 +0000