نتایج جستجو برای: angiofollicular

تعداد نتایج: 65  

Nouri, Gohar, Zahed Pasha, Shaghayegh, Abad, Mohsen , Hamidi, Seyed Hasan , Safdari, Mohammad Reza , Soltani, Hosseinali ,

Introduction: Angiofollicular lymph node hyperplasia (ALNH) or Castleman’s disease (CD) is an unusual benign non-neoplastic lymphoproliferative disease. CD can present as a localised mass. In this paper a rare case of Castleman’s disease in a 34 years old woman with a cervical mass is presented. Case Presentation: A 34 years-old woman presented in July 2018 with a painful mass neck that was app...

Journal: :Canadian journal of surgery. Journal canadien de chirurgie 2009
Jimmy Bejjani Bernard Lemieux Gilles Gariepy Rami Younan

An asymptomatic 29-year-old woman, with a long-term history of mild anemia, was referred to our hospital for evaluation. She was pale and asthenic. Except for anemia, her past medical and surgical history was unremarkable. There was no history of spoliation, and we noted no coagulopathy, type-B symptoms or systemic disease. Results of a complete physical examination were normal. The abdomen was...

Journal: :The Journal of the Association of Physicians of India 2008
Dinesh Kumar Rajni

Sir, Castleman’s disease, also known as Angiofollicular lymphnode hyperplasia is a rare disorder of lymphoreticular system with heterogenous clinical manifestations.1 Histopathologically, it has two variants1 hyaline vascular variant and plasma cell variant. While hyaline vascular variant usually present with localized yet marked lymphadenopathy2 with few constitutional symptoms, lymphoreticula...

Journal: :Journal of clinical and experimental hematopathology : JCEH 2014
Prasad R Koduri Mohammed Parvez Sashidhar Kaza Prabhakar Pappu Sekaran Anuradha

Angiofollicular lymph node hyperplasia, with the eponym Castleman disease (CD) is a histomorphologic entity uniting a group of diseases with related and occasionally overlapping pathogenesis. Histologic variants of CD include the hyalinevascular, plasmacytic, and mixed types and each of these may be clinically unicentric or multicentric. Recent reports describe a variant of idiopathic multicent...

Journal: :Blood 2004
Alice Berezne Félix Agbalika Eric Oksenhendler

Multicentric Castleman disease (MCD) is a distinct lymphoproliferative disorder characterized by lymphadenopathy with angiofollicular hyperplasia and plasma cell infiltration. Patients typically have fever associated with lymphadenopathy, hepatosplenomegaly, respiratory symptoms, peripheral edema, cytopenia, hypergammaglobulinemia, hypoalbuminemia, and high levels of serum C reactive protein (C...

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