Results 61 to 70 of about 317,416 (245)

New Aspects of Thromboangiitis obliterans (von Winiwarter-Buerger's Disease) [PDF]

open access: yes, 1984
The existence of thromboangiitis obliterans as a clinical entity has been a matter of debate for many years. In contrast to other immunovasculitides there is no organ involvement while peripheral vessels are affected.
Berlit, Peter   +3 more
core   +1 more source

A Retrospective Histopathological Study of Cutaneous Granulomatous Diseases at A Tertiary Dermatology Center in Kuwait [PDF]

open access: yes, 2023
Background: Granulomatous inflammation is a common histological pattern observed in skin biopsy. Due to the overlapping histological features produced by different etiological agents, granulomatous inflammation poses a diagnostic problem for ...
Rawan Almutairi*, Humoud Al-Sabah
core   +1 more source

Gingival Juvenile Xanthogranuloma [PDF]

open access: yes, 2019
Juvenile xanthogranuloma (JXG) is a benign histiocytosis that occurs in the pediatric population. Cutaneous JXG is the most common form, while extracutaneous lesions, including oral JXG, is extremely rare.
김동욱   +8 more
core   +1 more source

Congenital Juvenile Xanthogranuloma of Foot, a Nodular Lesion: An Unusual Case in 2-month-old Infant [PDF]

open access: yes, 2021
A 2-month-old infant presented with a circumscribed nodule on left foot since birth. Excision biopsy showed juvenile xanthogranuloma, an uncommon diagnosis in an unusual site; common sites being head and neck.
Anand K Verma   +4 more
core   +1 more source

Surgical Treatment for Adult-Onset Limbal Xanthogranuloma: A Case Report with 4-Year Follow-Up

open access: yesCase Reports in Ophthalmology, 2022
Xanthogranuloma is a benign histiocytic disorder that generally appears in infants and children and often called juvenile xanthogranuloma (JXG). Typical reddish-yellow cutaneous papules or nodules are the most common presentation of JXG.
Pichaya Chuephanich   +3 more
doaj   +1 more source

Neonatal Systemic Juvenile Xanthogranuloma with an Ominous Presentation and Successful Treatment [PDF]

open access: yes, 2011
This case report originated from a case of neonatal multisystemic juvenile xanthogranuloma (JXG). The patient presented with blue muffin rush, cervical mass, bone destruction, lung nodule, hepatosplenomegaly, and coagulopathy and was successfully treated
Fan, Rong, Sun, Jihong
core   +2 more sources

Endoscopic treatment of mediastinal pancreatic pseudocyst using lumen apposing metal stents - Case report [PDF]

open access: yes, 2023
Mediastinal pancreatic pseudocyst (PP) is a rare complication of acute alcoholic pancreatitis. Endoscopic drainage has become widely used in the management of PPs and novel lumen apposing metal stents (LAMS) could provide more effective ...
Kralj, Dominik   +2 more
core   +2 more sources

Juvenile Xanthogranuloma Presenting as Bilateral Non-Infiltrative Extraconal Superior Orbital Tumour in a 27 Year Old Nigerian Woman: Features, Management and Outcome

open access: yesClinical Medicine Insights: Case Reports, 2012
Introduction Orbital masses in adults are often caused by systemic diseases or are associated with systemic manifestations. Juvenile xanthogranuloma as a cause is rare and unreported in Africa.
Okosa Michael Chuka   +1 more
doaj   +1 more source

Juvenile Xanthogranuloma in Vulva of a 10-Year-Old Child [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
A 10-year-old child presented with asymptomatic, well-circumscribed nodule in the vulva. Excision biopsy showed features of classic Juvenile Xanthogranuloma (JXG) which is a rare benign disorder of non-langerhans’ cell group of histiocytic proliferative
Barkha Gupta   +3 more
doaj   +1 more source

Neoadjuvant intralesional methotrexate for juvenile xanthogranuloma in an adult [PDF]

open access: yes, 2021
Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis usually occurring in infants and typically located in the head or neck.1 Clinically, solitary skin lesions are found in 60%–82% of patients and the most common variant is characterized
Antoñanzas, J. (Javier)   +6 more
core   +1 more source

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