Results 41 to 50 of about 6,363 (176)
American Journal of Roentgenology, 1983 The value of computed tomography (CT) in distinguishing among mediastinal fatty tumors, vascular abnormalities, and fluid-filled cystic masses is well established. However, little has been written about the use of CT to identify mediastinal masses with soft-tissue characteristics nor of the ability of CT to assess the degree of enhancement of these ...
G, Onik, P C, Goodman
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Immunophenotypic characteristics of plasma cells in POEMS syndrome
Cytometry Part B: Clinical Cytometry, EarlyView.Abstract To analyze the immunophenotypic characteristics of plasma cells in patients with polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes (POEMS) syndrome. This retrospective study included patients with POEMS syndrome hospitalized in the Department of Hematology, Huashan Hospital, from September 2017 to August 2025 ...
Zhenhua Wang +6 more
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Persistent or recurrent Castleman′s disease - Look out for a lurking lymphoma!
Indian Journal of Medical and Paediatric Oncology, 2011 Castleman′s disease, a rare condition of uncertain etiology clinically presents in isolated form or as a multicentric disease. The multicentric form can develop malignancies such as Kaposi′s sarcoma or lymphomas.
Shalinee Rao +4 more
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SAGE Open Medical Case Reports, 2022 Castleman disease is a heterogeneous group of disorders of lymphoid tissue. It can often mimic other autoimmune diseases or malignancies, presenting a diagnostic dilemma to attending clinicians.
KUIS Gunathilake +4 more
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Respirology, EarlyView.We assessed the diagnostic yield of EBUS‐guided transbronchial mediastinal cryobiopsy (EBUS‐TBMC) compared with EBUS‐transbronchial needle aspiration (EBUS‐TBNA) in patients with suspected mediastinal lymphoproliferative disorders (LPDs). EBUS‐TBMC was superior to EBUS‐TBNA and achieved a high diagnostic yield in patients with suspected mediastinal ...
Yaniv Dotan +12 more
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Multicentric Castleman's Disease [PDF]
Medical Journal Armed Forces India, 2002 Castleman's disease is a rare, atypical lymphoproliferative disorder that is morphologically and clinically heterogeneous and is associated with a risk of developing malignant lymphoma. It represents a distinct form of lymph node hyperplasia rather than a neoplasm or a hamartoma. In Castleman's original report, this lesion was described as solitary and
M K, Gupta, S K, Magu, A, Behl
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Incidentally detected Castleman disease in a patient with allergic rhinosinu sitis [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2008 INTRODUCTION Castleman disease was for the first time described in 1956 as a mediastinal tumour mass. Etiology of this disease is still unknown. The disease can be solitary and multicentric or rarely of a mixed type.
Stojšić Jelena +4 more
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It's Not You, It's the System: Women Professors in TESOL and the Persistence of Gender Bias
TESOL Quarterly, EarlyView.Abstract Although progress has been made with respect to the role and position of women in academia, overt and covert discrimination as well as structural and systemic bias persist. In this article, we report on research conducted with 14 women professors from 10 different countries to explore to what extent these issues affect women professors in ...
Sarah Mercer +3 more
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Step into action: how reminders shape engagement in fitness apps
Economica, EarlyView.Abstract Regular exercise offers well‐documented health benefits, and mobile applications are increasingly used to promote physical activity. In this study, we conduct a large‐scale randomized controlled trial with 20,187 users of the WeWard app in France to evaluate the effectiveness of different message framings and intervention durations on app ...
Beatrice Braut +2 more
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Refractory Castleman's Disease
Hematology, 1998 Angiofollicular lymph node hyperplasia is an uncommon low-grade lymphoproliferative disorder first described by Castleman. It is typically asymptomatic with diagnosis incidentally made in young males on chest radiology. Biopsy, in 90% of cases, shows the hyaline vascular variant.
P, Jacobs, L, Wood, V, Jogessar
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