نتایج جستجو برای: castleman disease

تعداد نتایج: 1490199  

Journal: :Gynecology Obstetrics & Reproductive Medicine 2016

Journal: :American Journal of Clinical Pathology 2013

2010
Hossein Karami Alireza Alam Sahebpour Maryam Ghasemi Hasan Karami Mojdeh Dabirian Kurosh Vahidshahi Farzad Masiha Soheila Shahmohammadi

BACKGROUND Castleman's disease or angiofollicular lymphoid hyperplasia is a rare benign lymph node hyperplasia usually presenting as an asymptomatic mediastinal mass in children. The disease can present at any extra thoracic site with lymphoid tissue such as retroperitoneal, mesentery, axilla, and pelvis. Hepatic localization castleman disease is very rare in children. Herein, we reported a cas...

Journal: :Journal of clinical pathology 1999
J L Dargent J Delplace C Roufosse J P Laget L Lespagnard

A nine year old boy with localised Castleman disease of the hyaline-vascular subtype developed a calcifying fibrous pseudotumour. This pathological association does not appear to have been described before. In this case, the development of this very unusual soft tissue tumour-like process was thought to be related to a previous fine needle aspiration biopsy, which was performed because of lymph...

2017
Farnaz Shariati Elizabeth Verter Wendy Chang Li Huang Virendra Joshi

Unicentric Castleman disease is a rare condition of lymphoid hyperplasia, of which only 15% of cases occur in the abdomen. We report a 66-year-old man who presented with complaints of abdominal pain. Computed tomography scans revealed nephrolithiasis and a homogeneous calcified mass between the pancreas and stomach and several para-pancreatic nodes. Direct visualization during exploratory lapar...

Journal: :Journal of clinical and experimental hematopathology : JCEH 2013
Yasufumi Masaki Akio Nakajima Haruka Iwao Nozomu Kurose Tomomi Sato Takuji Nakamura Miyuki Miki Tomoyuki Sakai Takafumi Kawanami Toshioki Sawaki Yoshimasa Fujita Masao Tanaka Toshihiro Fukushima Toshiro Okazaki Hisanori Umehara

Multicentric Castleman's disease (MCD) is a polyclonal lymphoproliferative disorder that manifests as marked hyper-γ-globulinemia, severe inflammation, anemia, and thrombocytosis. Recently, Takai et al. reported a new disease concept, TAFRO syndrome, named from thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly. Furthermore, Kojima et al. reported Japanese MCD cases with ef...

2011
Luciana Wernersbach Pinto Estevão Portela Nunes

Both multicentric Castleman disease and Kaposi sarcoma are more frequently observed in HIV infected patients. The coexistence of these Human herpesvirus 8 related lesions, in the same tissue, has been observed, but literature reports are scant. On the other hand, the expression of HHV-8-LANA-1 is easily demonstrable by immunohistochemistry. This has been shown to be a powerful tool for the diag...

2017
Hui Huang Ruie Feng Jian Li Xinyu Song Shan Li Kai Xu Jian Cao Lu Zhang Yalan Bi Zuojun Xu

Intrathoracic involvement is common in Castleman disease (CD), but CD-associated diffuse parenchymal lung disease (DPLD) is rare and not well-reported.We conducted a retrospective analysis of 262 CD patients with a definite pathological diagnosis who were hospitalized between 1999 and 2015.Twenty-two CD patients had DPLD based on chest computed tomography (CT) scans. Among them, 9 were male and...

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