نتایج جستجو برای: rare case

تعداد نتایج: 1492855  

Journal: :archives of trauma research 0
yuk chuen siu department of orthopaedics and traumatology, north district hospital, sheung shui, china tun hing lui department of orthopaedics and traumatology, north district hospital, sheung shui, china; department of orthopaedics and traumatology, north district hospital, sheung shui, china. tel: +86-85226837588, fax: +86-85226837588

conclusions bilateral anterior shoulder dislocation is very rare. the excessive traction force during closed reduction may lead to nerve palsy. clear documentation of neurovascular status and adequate imaging before and after a reduction should be performed. introduction unilateral anterior shoulder dislocation is one of the most common problems encountered in orthopedic practice. however, simu...

2017
Belide Shruthi B.R. Nilgar Anita Dalal Nehaben Limbani

Harlequin ichthyosis is a very rare condition that affects the skin of newborns. It is associated with poor barrier function of the skin leading to dehydration and leaves newborns prone to infections. It is due to mutations in adenosine triphosphate binding cassette A12 gene transmitted as an autosomal recessive disorder. The prognosis is very poor in these cases. Here, we report one such rare ...

Journal: :Annals of the Academy of Medicine, Singapore 2004
S C Maniangatt J N Panicker M Thomas K Pavithran

INTRODUCTION Congenital erythropoietic porphyria is one of the rare forms of an intriguing group of metabolic disorders known as porphyrias. Less than 200 cases have been reported in the literature. CLINICAL PRESENTATION We report the case of a 27-year-old gentleman who had the clinical profile suggestive of porphyria, now presenting with anaemia. The type of porphyria was found to be congeni...

AHMAD KHOSSRAVY, MANOOCHEHR M. LARI, TAGHI GHIASSI,

This is the first documented case of esophageal carcinoma in a 14 year old boy which has been reported to date. Carcinoma of the esophagus is rare before the third decade. The present case highlights the fact that the condition should be kept in mind in the differential diagnosis of progressive dysphagia even in children and teenagers

Journal: :iranian journal of otorhinolaryngology 0
ranga reddy department of otorhinolaryngology, kamineni institute of medical sciences, india ankit singhania department of otorhinolaryngology, sbks medical institute and research centre, india ajay george department of otorhinolaryngology, sbks medical institute and research centre, india ranjan kumar department of otorhinolaryngology, kamineni institute of medical sciences, india sanjay kumar department of otorhinolaryngology, kamineni institute of medical sciences, india

introduction: castleman's disease is a rare lymphoproliferative disorder which may be confused with other causes of lymphadenopathy. case report: here we report a case of unicentric castleman's disease presenting with cervical lymphadenopathy. the patient was treated with complete surgical excision of lesion and was disease free at the time of reporting this article. this case has bee...

Journal: :iranian journal of otorhinolaryngology 0
ganakalyan behera department of otorhinolaryngology and head neck surgery, all india institute of medical sciences, saket nagar, bhopal, madhya pradesh, india. dillip samal department of otorhinolaryngology and head neck surgery, all india institute of medical sciences, saket nagar, bhopal, madhya pradesh, india.

introduction: fibrolipoma, a subtype of lipoma is painless, well-circumscribed, slow-growing, submucosal benign adipocyte tumour. it is uncommon in the oral cavity and oropharyngeal region, with rare incidence in the retropharynx even rarest in pediatric age group.   case report: a very unusual case of fibrolipoma is presented in a pediatric patient, who had a huge retropharyngeal fibrolipoma a...

Introduction: Necrotizing sialometaplasia is a rare, benign, and self-limiting inflammatory lesion that commonly involves minor salivary glands. It is theoretically associated with ischemia. It is commonly found in the palate, and laryngeal presentation is a very unusual entity. Almost half of such cases have an underlying malignancy; therefore, suspicion of a malignant lesion should be high wh...

Background: The outbreak of coronavirus disease 2019 (COVID-19) has become a global crisis, as the World Health Organization (WHO) declared COVID-19 as a global pandemic. Complete heart block, resulting from an abnormal heart rhythm, is a rare presentation of this infection, which can be life-threatening due to possible progression into ventricular tachycardia. Case Presentation: We report a c...

Oveis Salehi Saleh Mohebbi, Sedighe Ebrahimpoor

Introduction: Nasal teeth eruption is a rare phenomenon. The variability of symptoms and generic history makes the diagnosis difficult. This difficulty is more challenging when the tooth is placed in the depth of septum.   Case Report: Our case is an example of this problem. Herein, we present a case of intraseptal tooth with nasal obstruction and septal deviation and recurrent sinusitis. We p...

توکل نیا, دکتر رحیم, دژآباد, دکترولی ,

ABSTRACT Complete absence of one kidney is a relatively rare finding that is assosciated with genital anomalies in one third of cases. This case at first was referred to urologist as a Case of pelvic ectopic kidney, but after complementary investigations, the patient was operated by urologist and gynecologist together as a case of didelphic uterus with Hematosalpinx. The clinician should eval...

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