نتایج جستجو برای: herein

تعداد نتایج: 64426  

Herein, we present the case of a 45-year-old woman with pulsion and midesophageal diverticula, who had complaints of dysphagia and regurgitation. Diagnosis was confirmed by endoscopy and barium swallow. The patient underwent right posterolateral thoracotomy with excision of diverticula and repair of the muscular layer along the site of diverticula. Five days following the operation, barium swal...

Dabiri Shahriar Meymandi Simin Shamsi Shafiei Hamidreza

Epidermolysis Bullosa Puriginosa is a genetic mechanobullous disease characterized by pruritus, lichenified or nodular prurigo-like lesions, occasional trauma-induced blistering, excoriations, milia, nail dystrophy and albopapuloid lesions that appear at birth or later. Scarring and prurigo are most prominent on the shins. Herein, we report a case with a history of blisters since childhood foll...

A Asilian S Karbasioun

Herein we report a 6-year-old Afghans patient referred to Department of Dermatology, St. AL-Zahra Hospital in Isfahan with ulcerative and nodular lesions disseminated over the face, arms, buttocks, pelvic girdle and legs in 2002. Direct smears of the lesions were positive for Leishman bodies. Leishmanin skin test was negative. He also had dactylitis in some digits and toes. PCR from bone biopsy...

AR Firoozjahi M Adabi M Ghasemi

Lyme disease is caused by the spirochete Borrelia burgdorferi. Depending on the stage of illness, infection may be limited to the skin or involve the cardiac, nervous and musculoskeletal systems. Herein, we report a case of Lyme disease in a 23-year-old woman from North of Iran (Mazandaran) in early-localized stage of erythema chronicum migrans. The diagnosis was confirmed by the presence of se...

MR Mortazavi

Localized scalp hair loss has different causes which alopecia areata, trichotillomania, tinea capitis and early lupus erythematosus are the most important ones. There are several reports of localized alopecia after tick and flea bites and bee stings, but there is only one report of ant-induced alopecia in the literature. We report herein two cases of alopecia induced by ants of genus Phei...

Journal: :journal of research in medical sciences 0
babak tamizifar golnaz samadi maryam rismankarzadeh

hemophagocytic syndrome (hps) is an uncommon manifestation in systemic lupus erythematosus (sle). clinical features of hps include fever, pancytopenia, abnormal liver enzyme, hepatosplenomegaly, lymphadenopathy, and coagulation disorder. hps comprises primary and reactive forms. herein, we describe a case of untreated sle with hps as one of the first manifestations of systemic lupus.

Journal: :iranian journal of radiology 0
hee young choi department of radiology, graduate school, kyung hee university, seoul, korea ji hye jang department of radiology, college of medicine, kyung hee university hospital, kyung hee university, seoul, korea kyung mi lee department of radiology, college of medicine, kyung hee university hospital, kyung hee university, seoul, korea woo suk choi department of radiology, college of medicine, kyung hee university hospital, kyung hee university, seoul, korea sang hoon kim department of otolaryngology, college of medicine, kyung hee university hospital, kyung hee university, seoul, korea seung geun yeo department of otolaryngology, college of medicine, kyung hee university hospital, kyung hee university, seoul, korea

primary nasopharyngeal tuberculosis (tb) without pulmonary involvement is rare, even in endemic areas. herein, we present a rare complication of primary nasopharyngeal tb accompanied with tuberculous otomastoiditis (tom) and ipsilateral facial nerve palsy, in a 24-year-old female patient, with computed tomography and magnetic resonance imagery findings.

Journal: :iranian journal of allergy, asthma and immunology 0
mojgan safari seyed hesamedin nabavizadeh sara kashef

acute renal failure is one of the side effects while using intravenous immunoglobulins. this complication is also observed with iodinated contrast media. herein, we describe a patient with acute renal failure who received intravenous immunoglobulins and iodinated contrast media concomitantly. both drugs are responsible for osmotic nephrosis. the same effect on renal cells may explain a synergis...

Journal: :iranian journal of blood and cancer 0
peyman eshghi pediatric congenital hematologic disorders research center, mofid children hospital, shahid beheshti university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mohammad kajiyazdi pediatric congenital hematologic disorders research center, mofid children hospital, shahid beheshti university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mohammad hammoud pediatric congenital hematologic disorders research center, mofid children hospital, shahid beheshti university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

congenital factor x deficiency is a rare autosomal recessive bleeding disorder that presents with variable bleeding tendency and prolonged coagulation tests, prothrombin time, and partial thromboplastin time. thromboembolic events have not been reported in patients with factor x deficiency yet. herein, we report a patient with factor x deficiency who had recurrent venous thromboembolic events.

Journal: :iranian journal of medical sciences 0
s. shamsadini department of dermatology, kerman university of medical sciences m. hyatbakhsh abbasi department of internal medicine, kerman university of medical sciences m.h. bagheri kashani department of dermatology, kerman university of medical sciences

nekam's disease is a rare dermatosis characterized by a distinctive seborrheic dermatitis with prominent facial eruption.  it is further associated with violaceous, papular, and/or nodular lesions on the extremities and trunk, typically arranged in a linear and reticulate pattern.  herein, describe a patient with nekam's disease, which resembled darier’s disease in clinical manifestation.  the ...

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