Histiocyte-rich ROS1-rearranged inflammatory myofibroblastic tumour of the trachea: A rare neoplasm presenting with asthma-like symptoms. [PDF]
A flow volume loop demonstrated classical upper airway obstruction pattern. Abstract Inflammatory myofibroblastic tumour is a rare tumour. We present an atypical case of Inflammatory myofibroblastic tumour which was trachea in location, histocyte rich and ROS1 rearranged.
Kwok CT+5 more
europepmc +2 more sources
Juvenile Xanthogranuloma as Differential Diagnosis of a Vulvar Mass: A Case Report
Vulvar masses in children are an unusual finding but their differential diagnosis is extensive. In case of solid masses, rhabdomyosarcoma (RMS) must always be considered due to the fact that it is the most common tumor in external genitals during ...
I. Bada Bosch+7 more
semanticscholar +1 more source
C.E. Credit. Xanthogranuloma of the Palate in an Adult: A Case Report with Differential Diagnosis
Background Solitary oral mucosal xanthogranuloma, previously termed juvenile xanthogranuloma, is exceedingly rare in adults. Extracutaneous lesions are similarly rarely seen; and the condition generally affects infants and children.Methods This case ...
Hardev M. Singh+3 more
doaj +1 more source
NTRK expression is common in xanthogranuloma and is associated with the solitary variant
Abstract Background Previously identified mutually‐exclusive driver genes in juvenile xanthogranuloma (JXG) and adult xanthogranuloma (AXG) include mutations in MAP kinase pathway genes such as MAP2K1, BRAF, ARAF, KRAS, NRAS, PIK3CD as well as fusions in BRAF and ALK, with a subset of cases with no identified driver yet. NTRK fusion has been identified
B. Umphress+6 more
wiley +1 more source
Congenital Giant Juvenile Xanthogranuloma, Let It Be.
Description Juvenile xanthogranuloma (JXG) is a rare type of non-Langerhans cell histiocytosis. JXGs are benign and have a self-limiting course generally lasting 6 months to 3 years, with some reported durations longer than 6 years.
M. Carletti+3 more
semanticscholar +1 more source
Juvenile Xanthogranuloma of the Nose [PDF]
Juvenile xanthogranuloma is a type of non-Langerhans cell histiocytosis that occurs most frequently in infants and children. It is usually asymptomatic and can present as either a cutaneous or extracutaneous lesion. The present case is believed to be the first reported in the English literature of juvenile xanthogranuloma presenting as an ulcerated ...
Hisham Aburezq+3 more
openaire +3 more sources
Cutaneous findings in neurofibromatosis type 1 [PDF]
Neurofibromatosis type 1 (NF1) is characterized by major and minor cutaneous findings, whose recognition plays a key role in the early diagnosis of the disease.
Argenziano G.+4 more
core +1 more source
New Aspects of Thromboangiitis obliterans (von Winiwarter-Buerger's Disease) [PDF]
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]
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]
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