نتایج جستجو برای: necrobiotic xanthogranuloma

تعداد نتایج: 649  

Journal: :Asploro Journal of Biomedical and clinical Case Reports 2021

Multiple adult xanthogranuloma (MAXG) is an uncommon form of xanthogranuloma. The clinical manifestation MAXG relatively rare, but it has characteristic histopathological and immunohistochemical features. mainly associated with cutaneous damage, extracutaneous manifestations such as cervical spine, intracardiac, periocular lesions have rarely been reported. In patients systemic association, cli...

2011
Hiroyuki Kinoshita Shunsuke Yamaguchi Yoshifumi Sakata Kazuo Arii Kazunari Mori Rieko Kodama

BACKGROUND Xanthogranuloma of the stomach is an extremely rare disease, and this lesion has only been found to coexist with early gastric cancer in 2 cases in the literature. CASE PRESENTATION We report a case of xanthogranuloma of the stomach combined with early gastric cancer that mimicked an advanced stage tumor. A 65-year-old female was referred to our hospital because of epigastralgia. D...

2011
Alessandro Villa Umberto Mariani Francesco Villa

INTRODUCTION Juvenile xanthogranuloma is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. The presence of single or multiple raised cutaneous lesions characterize this self-healing disorder. Extracutaneous sites are rare. CASE PRESENTATION We present a rare case of oral juvenile xanthogranuloma in a 49-year-old Caucasian woman. The histopatholog...

Journal: :The Canadian journal of plastic surgery = Journal canadien de chirurgie plastique 2008
M Amir Mrad Kevin Chan Tatiana Ks Cypel Ronald M Zuker

Juvenile xanthogranuloma is a relatively uncommon, benign histiocytic proliferative disorder. A case of juvenile xanthogranuloma in a 13-month-old girl with an unusual clinical form is described. She presented with a yellow-red projecting nodule over the helical rim of her right ear. The lesion was histologically diagnosed as juvenile xanthogranuloma after excisional biopsy. Although primarily ...

2017
Sushmita Pradhan Shuang Chen Lin Xiong

Juvenile xanthogranuloma is an unusual, self-limiting dermatological disorder occurring especially in infants, late childhood and rarely in adults. It belongs to the broad group of non-Langerhans cell histiocytosis. It usually appears as solitary or multiple papules, macules or nodules several millimeters in diameter with the head and neck being the most common site of involvement and vulva bei...

مصطفی میرشمس شهشهانی, , کاترین کیاوش, ,

Background: Juvenile xanthogranuloma is a benign, normolipemic, dendrocytic histiocytosis that usually affects young children. It presents clinically as single or multiple yellow-brown papulonodular lesions in the upper part of the body, especially the head and neck. In adults, xanthogranuloma is not common and usually presents as a single lesion. Multiple xanthogranuloma in adults is rare. For...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2014
Henry H W Lau Wilson W K Yip Allie Lee Connie Lai Dorothy S P Fan

Three cases of juvenile xanthogranuloma from two ophthalmology departments were reviewed. Clinical histories, ophthalmic examination, physical examination, investigations, and treatment of these cases are described. A 4-month-old boy presented with spontaneous hyphema and secondary glaucoma. He was treated with intensive topical steroid and anti-glaucomatous eye drops. The hyphema gradually res...

2010
Fumiaki Shimizu Hiroko Taneda Haruaki Sato Aiko Kato Naoko Takeo Sakuhei Fujiwara

Orbital xanthogranuloma is an uncommon tumor. It is usually associated with a systemic or hematological disease. This report presents a rare case of orbital xanthogranuloma associated with heart disease and thrombocytopenia. A 52-year-old female presented with a bilateral periorbital subcutaneous tumor that had existed for 3 years. Although immunoglobulin levels were within the normal limits, t...

Journal: :Neurologia medico-chirurgica 2011
Yuuta Kamoshima Yutaka Sawamura Hiroaki Motegi Kanako Kubota Kiyohiro Houkin

Five Japanese children presented with rare xanthogranuloma located in the sellar region between 2000 and 2010 at the Department of Neurosurgery, Hokkaido University Hospital. Endocrinological examination disclosed central diabetes in four patients. Preoperative magnetic resonance (MR) imaging and computed tomography (CT) demonstrated clearly defined intra- or suprasellar masses appearing as iso...

Journal: :The British journal of ophthalmology 1993
I Casteels J Olver M Malone D Taylor

Five infants with biopsy proved juvenile xanthogranuloma of the iris were reviewed. Early treatment with subconjunctival injection of steroids and topical steroid drops resulted in regression of the lesion in four patients. One patient, reviewed at the age of 8 months after glaucoma which had developed secondary to the iris xanthogranuloma, had been treated by surgery alone: the visual outcome ...

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