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Case Report: Toxic epidermal necrolysis in hemodialysis patient |
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Uday Venkat Mateti, Shankar Prasad Nagaraju, Manohar Bairy, Ravindra Prabhu Attur, Anantha Naik Nagappa, Anuradha Calicut Kini Rao Adv Biomed Res 2015, 4:63 (27 February 2015) DOI:10.4103/2277-9175.152119 PMID:25821763Toxic epidermal necrolysis (TEN) is a rare and life-threatening allergic drug reaction. We report a 26-year-old young female with end-stage renal disease on maintenance hemodialysis developing TEN while on filgrastim and phenytoin. It was successfully treated with intravenous immunoglobulins and steroids. |
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Case Report: Life-threatening misdiagnosis of bulbar onset myasthenia gravis as a motor neuron disease: How much can one rely on exaggerated deep tendon reflexes |
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Keivan Basiri, Behnaz Ansari, Ali Asghar Okhovat Adv Biomed Res 2015, 4:58 (23 February 2015) DOI:10.4103/2277-9175.151874 PMID:25802827The autoimmune disease myasthenia gravis (MG), can mimic a variety of neurological disorders leading to a delay in diagnosis and treatment. On occasions, misdiagnosis of MG could lead to unnecessary therapeutic interventions. We report the case of a 50 year-old man, in whom MG was mistaken for motor neuron disease (MND). Subsequently, correct diagnosis and optimal management resulted in saving his life and significant improvement in his functional status. We discuss the importance of considering MG as one of the potential differential diagnoses among cases of new onset or recurrent unexplained bulbar symptoms, despite exaggerated deep tendon reflexes. Also, a literature review on the misdiagnosis of MG and the potential pitfalls in MG diagnosis are discussed. |
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Case Report: Peripheral communications of intercostobrachial nerve Peripheral communications of the intercostobrachial nerve in relation to the alar thoracic artery |
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Shaifaly Madan Rustagi, Mona Sharma, Nidhi Singh, Vandana Mehta, Rajesh K Suri, Gayatri Rath Adv Biomed Res 2015, 4:51 (17 February 2015) DOI:10.4103/2277-9175.151555 PMID:25802820The intercostobrachial nerve (ICBN) is often encountered during axillary dissection for axillary lymph node dissection (ALND) for diagnostic and therapeutic surgery for mastectomy. The present report is a case observed in the Department of Anatomy at Vardhman Mahavir Medical College, Delhi during routine dissection of the upper extremity of a male cadaver for first year undergraduate medical students. On the right side , the medial cord of brachial plexus gave two medial cutaneous nerves of arm. Both the nerves were seen communicating with the branches of the ICBN. The ICBN and one of its branches were surrounding the termination of an alar thoracic artery. These peripheral neural connections of the ICBN with the branches of the medial cord can be a cause of sensory impairment during axillary procedures done for mastectomy or exploration of long thoracic nerves. The alar thoracic artery found in relation to the ICBN could further be a cause of vascular complications during such procedures. |
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Case Report: Frontotemporal dementia parkinsonism: Clinical findings in a large Iranian family |
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Keivan Basiri, Behnaz Ansari, Rokhsareh Meamar Adv Biomed Res 2015, 4:37 (11 February 2015) DOI:10.4103/2277-9175.151242 PMID:25789263Frontotemporal dementia (FTD) is a group of neurodegenerative disorders characterized by atrophy of the frontal and temporal lobes. Clinical features suggestive of FTD include pre-senile onset before the age of 65, behavioral changes, social and interpersonal disinhibition, fluent and nonfluent aphasia, and loss of insight. FTD and parkinsonism linked to chromosome 17 (FTDP-17) was defined during the International Consensus Conference in Ann Arbor, Michigan in 1996. FTDP-17 is an autosomally dominant inherited condition. Most genotypic alterations do not correlate with clinical phenotypes. However, mutations affecting exon 10 splicing are associated with parkinsonism. In the present study, a male case with FTDP who presented with insidious onset of speech difficulty at a young age that was associated with signs of parkinsonism and a positive family history of FTD with MAPT gene mutation at exon 13 has been reported. |
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Case Report: Stenotrophomonas maltophilia: Complicating treatment of ESBL UTI |
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Simit Kumar, Maitreyi Bandyopadhyay, Mitali Chatterjee, Parthajit Banerjee, Sumon Poddar, Debarati Banerjee Adv Biomed Res 2015, 4:36 (11 February 2015) DOI:10.4103/2277-9175.151241 PMID:25789262Stenotrophomonas maltophilia (S. maltophilia) is a gram-negative bacillus emerging as an opportunistic, nosocomial pathogen associated with a high mortality rate. The organism has been shown to survive several biocides used in the hospital setting. Hospital water sources can serve as a reservoir for S. maltophilia. The transmission of S. maltophilia to susceptible individuals may occur through direct contact with the source or through the hands of health care personnel. S. maltophilia is usually resistant to third-generation cephalosporins, aminoglycosides and antipseudomonal penicillins. These microorganisms are intrinsically resistant to carbapenems, and exposure to these agents has been linked to selection of S. maltophilia. There have also been reports of the organism developing resistance to trimethoprim-sulfamethoxazole (TMP-SMX), which was initially considered as the drug of choice for S. maltophillia infections. We describe a case of nosocomial urinary tract infection (UTI) due to S. maltophilia in a diabetic patient, which the patient developed during treatment with meropenem for UTI due to Klebsiella pneumonia that was resistant to TMP-SMX. |
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