نتایج جستجو برای: lymphangioma circumscriptum

تعداد نتایج: 5586  

2013
Pradeep Kajal Kamal Nain Rattan Vivek S Malik Vipin Garsa

Lymphangioma is an extremely rare cause of scrotal swelling. We are reporting such a tumor in a one and half year old child presenting with a painless, progressive scrotal swelling. The mass was evaluated and excised completely. Histopathology confirmed it as Lymphangioma.

2005
Huseyin Ozdemir Ercan Kocakoc Zulkif Bozgeyik Bengu Cobanoglu

Retroperitoneal cystic lymphangioma is a rare congenital malformation. The majority of lymphangiomas are present at birth and nearly all present before the age of two years. We report a case of giant cystic retroperitoneal lymphangioma in a patient who first presented with symptoms at the age of 7, underwent surgery, and who then suffered a recurrent mass 11 years later.

Journal: :Journal of medical genetics 1991
G Krüger L Pelz H R Wiedemann

We present a male infant with cranial hemi-hypertrophy, a lymphangioma, a lipoma, and epidermal naevi. A diagnosis of Proteus syndrome was made. His father had had a large lymphangioma resected from the right side of the face as a child. We propose that Proteus syndrome has been transmitted from father to son.

2016
Rajesh N. Swarnakar Jetendra D. Hazarey Chetan Dhoble Bhavesh Vaghani Alaine S. Ainsley James F. Khargie Lorena Likaj

BACKGROUND Lymphangioma is an atypical non-malignant, lymphatic lesion that is congenital in origin. Lymphangioma is most frequently observed in the head and neck, but can occur at any location in the body. About 65% of lymphangiomas are apparent at birth, while 80-90% are diagnosed by two years of age. Occurrence in adults is rare, as evidenced by less than 100 cases of adult lymphangiomas rep...

Journal: :بینا 0
ماندانا کلیشادی m klishadi golestan university of medical sciences, golestan, iranگرگان- خیابان پنج آذر- بیمارستان پنج آذر- دفتر آموزش بالینی

orbital lynphangioma is a low-flow or no-flow vascular malformation. it is a congenital and isolated hemodynamic lesion in which the clinical presentation and onset are related to orbital, peri-orbital or intracranial involvement. in addition, history of previous trauma and upper respiratory tract infection are important predictor factors. high resolution mri, doppler ultrasound and ct-scan are...

Journal: :Ear, Nose & Throat Journal 2006

Journal: :Breast care 2010
Ravikanth Balaji Krishnankutty Ramachandran

BACKGROUND: The aim of this study was to report magnetic resonance imaging (MRI) features of cystic lymphangiomas of the breast. METHODS: MRI of the breast was performed using a phased-array double breast coil with a 1.5-T MR scanner. Routine T1 and T2 and post-contrast sequential imaging was performed. RESULTS: The MRI characteristics of cystic lymphangioma in the breast are described. CONC...

Journal: :Pediatrics and neonatology 2016
Claudio Olivieri Lorenzo Nanni Anna Maria De Gaetano Lucia Manganaro Claudio Pintus

Retroperitoneal lymphangioma is extremely rare. Although these neoplasms are benign, they can grow progressively with subsequent compression and infiltration of the adjacent structures. Surgical excision is demanding when the lesion surrounds vital structures and it is generally fraught with a high recurrence and morbidity rate. We report the case of a huge retroperitoneal lymphangioma in a new...

Journal: :Asian journal of surgery 2004
Rakesh Handa Ravi Kale Krishan K Upadhyay

Lymphangiomas are congenital malformations of the lymphatic system, and 90% have manifested by the end of the second year of life. While 75% of these are located in the cervical region, only 2% to 3% are associated with an intrathoracic extension. An isolated mediastinal lymphangioma without a cervical component is an uncommon occurrence. Presented here is an isolated mediastinal lymphangioma t...

2009
JK Olabanji AO Oladele OC Famurewa O Adejuyigbe SA Ademola

BACKGROUND Lymphangiomas occur most commonly in the head and neck region, while other sites are rarely affected. A combination of retroperitoneal and genital lymphangioma is very rare indeed. Though congenital, it may persist into adulthood due to missed diagnosis and inadequate or total lack of treatment. MATERIALS AND METHODS A report of a 22-year-old male student who presented with recurre...

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