نتایج جستجو برای: astrocytic hamartoma

تعداد نتایج: 8937  

Journal: :iranian journal of radiology 0
ahmadreza afshar department of orthopedics and hand surgery, urmia university of medical sciences, urmia, iran omid assadzadeh department of orthopedics and hand surgery, urmia university of medical sciences, urmia, iran afshin mohammadi department of radiology, urmia university of medical sciences, urmia, iran; department of radiology, urmia university of medical sciences, urmia, iran. tel: +98-4413455810, fax: +98-4412353561

lipofibromatous hamartoma (lfh) is an extremely rare benign tumor, which is characterized by an excessive infiltration of the epineurium and perineurium by fibroadipose tissues. a 27-year-old woman was diagnosed with left carpal tunnel syndrome (cts) due to (lfh) of the median nerve. lfh was diagnosed by mri and sonography; the characteristic ultrasonographic feature of lfh showed a good correl...

2017
Varun Chaudhary Dr Ami Jani

Lhermitte-Duclos disease (LDD) is a benign neoplasm of posterior fossa, involving cerebellum. It is also known as dysplastic cerebellar gangliocytoma. It is not a true neoplasm but a hamartoma. It can be either isolated finding or associated with Cowden (multiple hamartoma syndrome). adults.

2014
Alberto Pieretti Chin-Lee Wu Rafael V. Pieretti

We present the case of the youngest reported patient with a bladder hamartoma detected prenatally by ultrasonography. Bladder tumors in newborns are rare, but a hamartoma should not be discarded among the diagnostic possibilities when evaluating a fetus or a newborn with a polypoid bladder lesion.

Journal: :Postgraduate medical journal 2003
M J Brookes S Manjunatha C A Allen M Cox

Brunner's gland hamartomas are rare tumours of the duodenum. These lesions have previously been described as being benign, with no malignant potential. A case report is presented of a Brunner's gland hamartoma, whose histology revealed a focus of well marked epithelial dysplasia. This case suggests a dysplastic stage in the natural history of Brunner's gland hamartoma, and questions the maligna...

Journal: :Turkish journal of urology 2016
Richard Shepler Jack M Zuckerman Dean Troyer John B Malcolm

We report a case of an urachal hamartoma in a 30-year-old African American woman. The urachal lesion was excised with a robotic-assisted laparoscopic partial cystectomy. Pathologic analysis revealed cysts, smooth muscle, and ciliated epithelium consistent with a hamartoma. The patient recovered without complication. This case highlights an unusual pathology that is infrequently reported followi...

Journal: :Actas dermo-sifiliograficas 2007
C M Bernal-Mañas M A Isaac-Montero M C Vargas-Uribe R Ruiz-Pruneda J P Hernández-Bermejo

Rhabdomyomatous mesenchymal hamartoma is a rare congenital lesion which consists of randomly arranged striated muscle fibers interspersed with mesenchymal elements. We describe the clinical and histopathological features of a rhabdomyomatous mesenchymal hamartoma in a one year-old patient presenting a bilobulated lesion in the mid-cervical line. No associated congenital malformations were obser...

Background & Objective: Glioblastoma-multiforme is the high grade form of astrocytic tumors with a short survival time, which are the most common type of brain tumors. Therefore, finding new therapeutic options is essential. Cyclin D1 is expressed in some human malignancies and can be a potential target for therapeutic intervention. The aim of the present study was to determine...

Journal: :Cell metabolism 2017
Yalin Zhang Judith M Reichel Cheng Han Juan Pablo Zuniga-Hertz Dongsheng Cai

Central regulation of metabolic physiology is mediated critically through neuronal functions; however, whether astrocytes are also essential remains unclear. Here we show that the high-order processes of astrocytes in the mediobasal hypothalamus displayed shortening in fasting and elongation in fed status. Chronic overnutrition and astrocytic IKKβ/NF-κB upregulation similarly impaired astrocyti...

2015
Kei Tanaka Takashi Kishimoto Masayuki Ohtsuka Yukio Nakatani Masaru Miyazaki

We report a case of pancreatic hamartoma-like solitary fibrous tumor which was differentiated from pancreatic hamartoma with the detection of NAB2-STAT6 fusion, a specific mutation for solitary fibrous tumors. A pancreatic well-demarcated solid nodule, 21 × 17 mm, of 82-year-old man was surgically enucleated. Microscopic findings were close to a pancreatic hamartoma that consisted of sparsely d...

Journal: :Journal of clinical pathology 1959
J E GOODYEAR A J SHILLITOE

In pulmonary pathology the term "hamartoma " is most commonly applied to a group of tumours in adults which usually contain cartilage as a constituent and arise from connective tissue (Sutherland, Aylwin, and Brewin, 1953). Willis (1958) does not think such growths are named correctly and gives good reasons for regarding them as acquired mixed tumours. On the other hand the mass replacing the e...

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