Results 41 to 50 of about 22,424 (233)
Journal of Surgical Oncology, EarlyView.ABSTRACT Background and Objective The vascular groove (VG) is no longer considered a resection margin but rather a surface of involvement. The clinical significance of an isolated VG+ remains debated. Therefore, this study evaluates the impact of isolated VG+, with or without vein resection, on overall survival (OS) and disease‐free survival (DFS ...
Callie A. Hlavin +9 more
wiley +1 more source
下大静脈及び腸骨静脈血栓を伴った後腹膜線維症の1例 [PDF]
, 2002 53歳女.両下肢の腫脹と乏尿を主訴に当院受診, CT上両側水腎症と両側腸骨動脈を取り囲む辺縁不整な軟部組織陰影を認めた, 腎後性腎不全に対し両側ダブルJカテーテル留置, 造影CTにて下大静脈及び左腸骨静脈内に血栓を認め, また下大静脈造影及びMRアンジオグラフィー(MRA)にて左腸骨静脈閉塞を認めた.中心静脈血栓を伴う特発性後腹膜線維症と診断し, 経口よりプレドニゾロン及びワーファリン投与開始した.投与1ヵ月後のCT及びMRAで血栓の消失を認め, 水腎症は改善, 再発を認めていないA 53-year ...
Tanuma, Yasushi, Yokoo, Akifumi
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An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]
, 2016 Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F. +5 more
core +2 more sources
Expansion of the Phenotype of Lymphatic Anomalies Caused by Somatic Activating BRAF Variant
Pediatric Blood &Cancer, EarlyView.ABSTRACT Background The somatic activating variant in BRAF (p.V600E) was recently described as a novel cause of macrocystic head and neck lymphatic malformations in three individuals. Other recent studies profiling the genetic causes of more complex lymphatic anomalies identified this same pathogenic BRAF variant.
Michael D. Fox +11 more
wiley +1 more source
Malignancies and immunoglobulin G4‐related disease
Rheumatology &Autoimmunity, EarlyView.Immunoglobulin G4‐related disease (IgG4‐RD) is associated with increased cancer risk. Malignancies affect both IgG4‐RD involved organs, such as the lung, pancreas, bile duct, and prostate, and noninvolved organs, such as the gastrointestinal duct. B‐cell neoplasms constitute a proportion of the malignancies linked to this disease.
Jingna Li, Wen Zhang
wiley +1 more source
Rheumatology &Autoimmunity, EarlyView.Clinical perspectives and comparisons between immunoglobulin G4‐related disease and antineutrophil cytoplasmic antibody‐associated vasculitis. Abstract Both immunoglobulin (Ig) G4‐related disease (IgG4‐RD) and antineutrophil cytoplasmic antibody (ANCA)‐associated vasculitis (AAV) are systemic disorders that affect a wide range of organs.
Wenhuan Zeng, Mingxin Bai, Yanying Liu
wiley +1 more source
Allergy, EarlyView.ABSTRACT IgG4, the least abundant IgG subclass in humans, is increasingly recognised for its involvement in allergic and autoimmune pathologies. Its unique properties, such as the tendency to form half‐molecules (one heavy chain and one light chain) and its generally non‐inflammatory nature, distinguish it from other IgG subclasses.
Louisa Tedesco +8 more
wiley +1 more source
Successful mycophenolate mofetil therapy in nine patients with idiopathic retroperitoneal fibrosis [PDF]
, 2017 Objective. To assess the therapeutic benefit of mycophenolate mofetil (MMF) in retroperitoneal fibrosis (RF). Methods. MMF 2 g/day and prednisone 1 mg/kg were initiated in nine patients with radiological (9/9) and histological verification (2/9) of ...
Adler, S. +3 more
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Equine Veterinary Journal, EarlyView.Abstract Background Strangulating lipomata are the most common cause of small intestinal strangulating obstruction. Evaluation of histological features of pathological and non‐pathological lipomata, and the histological properties of omental and retroperitoneal fat have not been described.
Alexandra Gillen +3 more
wiley +1 more source
IgG4-related autoimmune disease : imaging findings [PDF]
, 2013 IgG4 autoimmune disease (or hyper IgG4 disease) is a relatively recently described systemic disease that is characterised by abundant infiltration of IgG4-positive plasma cells and lymphocytes with associated fibrosis leading to organ dysfunction ...
Vassallo, Pierre
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