نتایج جستجو برای: lipomatosis

تعداد نتایج: 1748  

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2010
Lorraine V Kalia Liesly Lee Suneil K Kalia Farhad Pirouzmand Mark J Rapoport Richard I Aviv Dan Mozeg Sean P Symons

Skeletal fluorosis is rare in NorthAmerica. It can present with back pain and extremity weakness. Immobilization of the spine and the extremity joints can occur. It is usually caused by abnormally increased oral fluoride intake over many years. Epidural lipomatosis is usually caused by idiopathic obesity or corticosteroid use. It has been linked to highly active antiretroviral therapy (HAART) f...

Journal: :Neurology 2015
Amy Wei Lin Timo Krings

Our patient was worked up for mild developmental delay associated with focal scalp alopecia at age 6, and was diagnosed with encephalocraniocutaneous lipomatosis (also known as Haberland or Fishman syndrome), a rare neurocutaneous syndrome characterized by skin lesions (most commonly focal alopecia with or without underlying lipoma), ocular lesions, and CNS anomalies. CNS anomalies are usually ...

Journal: :European surgical research. Europaische chirurgische Forschung. Recherches chirurgicales europeennes 2006
Y Xu R L Liu Z H Zhang W M Zhao Q C Yang

We report a relatively rare case of renal replacement lipomatosis presenting as a renal mass. Computed tomography revealed a predominantly low-density and roundish mass, with an irregular renal parenchyma, high-density calcification, and abundant low-density fat. The differential diagnosis before surgery was squamous cell carcinoma, teratoma, or angiomyolipoma of the kidney. The case was initia...

2014
Brijesh Thakur Sanjeev Kishore Aparna Bhardwaj Sandip Kudesia

Symptomatic diffuse submucosal intestinal lipomatosis is a rare entity. Also few cases of epidermal inclusion cyst of caecum have been reported in literature. Here, we are presenting a rare case of intestinal submucosal lipomatosis with coincidence of epidermal inclusion cyst of caecum and presumptively diagnosed as carcinoma of ileocaecal region during surgery in a 55 years old male. Both are ...

2007
Chi-Chen Hou Chia-Yang hong Wen-Sheng Tzeng Yu-Kang Chang Reng-hong Wu Chi-Chen hou

Intestinal lipomatosis is a rare disease entity. Few cases have been reported in the literature. It is often associated with characteristic CT findings, making a preoperative diagnosis possible. Here we report a 49-year-old male who suffered from progressive abdominal distension, epigastralgia, nausea and vomiting for 2 days. Plain abdominal radiograph showed distended small bowels. Abdominal C...

Journal: :Acta dermatovenerologica Croatica : ADC 2008
Vlatka Pandzić Jaksić Tajana Stoos Veić

Two patients with features of multiple symmetric lipomatosis type 2 are presented. This particular disorder with a characteristic distribution of fat should be considered on differential diagnosis of obesity. Besides being rare, it may occasionally be unrecognized, especially in females. The etiology remains unknown; however, the association with high alcohol consumption is very strong. Several...

2009
Ahmet Tekin Zekai Ogetman

Multiple symmetric lipomatosis (also known as Madelung's disease, Launois-Bensaude syndrome or benign symmetric lipomatosis) is a rare disease, the etiology of which is unknown. Multiple, symmetric, non-encapsulated lipomatous masses on the face, neck, upper arms, and upper trunk are typical in most cases. Five out of the 200 cases reported in the literature were the distal form of the disease;...

2016
Sinead Culleton Christen D Barras Hamed Asadi Seamus Looby Paul Brennan Hong Kuan Kok

The severity of seizures presenting to the emergency department ranges from benign to life threatening. There are also a wide number of possible etiologies. Computed tomography (CT) emergency imaging may be required at presentation to elucidate a possible cause and assess signs of intracranial trauma. This case describes a serious seizure episode in a young man while on holiday. A CT brain show...

Journal: :Journal of Gastric Cancer 2010

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