Results 71 to 80 of about 9,327,495 (300)

Unicentric castleman's disease located in the lower extremity: a case report [PDF]

, 2011
Background Castleman's disease is a rare form of localized lymph node hyperplasia of uncertain etiology. Although the mediastinum is the most common site of involvement, rare cases occurring in lymph node bearing tissue of other localization have been ...
A Slotwiner, B CASTLEMAN, DM Cronin, F van Rhee, Harald Günnel, I Tazi, Inga-Marie Schaefer, J Lee, K Cokelaere, M Hakozaki, MG De, Michael Korenkov, Stefan Schweyer, WC Chen   +13 more
core   +5 more sources

SUBMANDIBULAR CASTLEMAN'S DISEASE

International Journal of Clinical Practice, 2002
SUMMARYCastleman's disease is a rare benign lymphoid tumour of unknown aetiology, which usually appears as a solitary mediastinal mass. We report an unusual case of Castleman's disease, an asymptomatic submandibular mass in the lower jaw, and we discuss the computed tomography appearance.
S C, Chan, S H, Ng, K F, Lee, S P, Hao, Y C, Cheung, Y L, Wan   +5 more
openaire   +2 more sources

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
openaire   +2 more sources

Unicentric mixed variant castleman disease associated with intrabronchial plasmacytoma. [PDF]

, 2014
Castleman disease (CD), described as a heterogeneous lymphoproliferative disorder, can be divided into different subtypes according to clinical appearance (unicentric and multicentric form) and histopathological features (hyaline vascular, plasma cell ...
A Carbone, A Slotwiner, AR Keller, Attila Csekeő, B Castleman, BT Lin, D El Demellawy, DC Schlosnagle, DM Menke, DM Menke, DMP Cronin, ED Hsi, G Frizzera, Gergely Varga, GM Dores, György Balázs, György Losonczy, JB Arlet, Judit Csomor, K Nagai, K Yoshizaki, L Zhang, Lilla Tamási, M Chilosi, M Hakozaki, MQ Du, N Tsukamoto, Noémi Eszes, PA Hall, PG Murray, R Burger, S Curioni, S Wilkinson, SJ Brandt, T Radaszkiewicz, T Shuaipaj, T Terada, TW Muskardin, Veronika Müller, WB Bowne, X Sun, Y Aoki, Ágota Szepesi   +42 more
core   +1 more source

Neurological Peculiarities of POEMS Syndrome: Experience From a Brazilian University Center

Muscle &Nerve, EarlyView.
ABSTRACT Aim Polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS) syndrome is a rare paraneoplastic syndrome associated with significant neurologic morbidity. Better understanding of the manifestations of this disease is crucial to early diagnosis and improvement of prognosis.
Renan Fabri Rosenstein, Jose Pedro Soares Baima, Thales Dalessandro Meneguin Pereira, Gracia Aparecida Martinez, Carlos Otto Heise, Angelina Maria Martins Lino   +5 more
wiley   +1 more source

Intrathoracic Castleman disease

TURKISH JOURNAL OF MEDICAL SCIENCES, 2014
To analyze patients with Castleman disease who were diagnosed by surgery.We retrospectively investigated the postoperative pathological records of operations performed between January 1992 and December 2012 in our hospital. Files of 19 patients with the diagnosis of Castleman disease were analyzed.There were 13 male and 6 female patients with a mean ...
Karaoğlanoğlu, NURETTİN, Acar, LN, Gülhan, SŞ, Biçakçioğlu, P, Ağaçkiran, Y, Özkara, Ş, Kaya, S   +6 more
openaire   +3 more sources

Type I IFN response associated with mTOR activation in the TAFRO subtype of idiopathic multicentric Castleman disease.

JCI Insight, 2020
The TAFRO clinical subtype of idiopathic multicentric Castleman disease (iMCD-TAFRO) is a rare hematologic illness involving episodic disease flares of thrombocytopenia, anasarca, fever, reticulin myelofibrosis, renal dysfunction, and organomegaly (TAFRO)
R. Pai, A. S. Japp, Michael V. Gonzalez, R. Rasheed, M. Okumura, Daniel J. Arenas, S. Pierson, V. Powers, A. Layman, Charlly Kao, H. Hakonarson, F. van Rhee, M. Betts, T. Kambayashi, D. Fajgenbaum   +14 more
semanticscholar   +1 more source

HHV‐8/KSHV in Solid Organ Transplantation: Current Gaps of Knowledge and Future Directions

Transplant Infectious Disease, EarlyView.
Risk mitigation strategies, including donors/recipients screening, DNAemia monitoring in recipients at risk, CNI‐to‐mTOR inhibitors switch, antivirals, and rituximab for KICS, may mitigate the impact of HHV‐8/KSHV infection in SOT. This review provides an update on KICS, identifies research gaps, and summarizes advances in screening and management ...
Alessandra Mularoni, Andrea Cona, Malgorzata Mikulska, Francesca Pecoraro, Carlotta Piazza, Elda De Vita, Giada Pietrosi, Matteo Bulati, Tiziana Lazzarotto, Mario Luppi   +9 more
wiley   +1 more source

Increased mTOR activation in idiopathic multicentric Castleman disease.

Blood, 2020
Idiopathic multicentric Castleman disease (iMCD) is a rare and poorly-understood hematologic disorder characterized by lymphadenopathy, systemic inflammation, cytopenias, and life-threatening multi-organ dysfunction.
Daniel J. Arenas, Katherine Floess, D. Kobrin, R. Pai, M. B. Srkalovic, M. Tamakloe, R. Rasheed, Jasira Ziglar, J. Khor, Sophia A T Parente, S. Pierson, D. Martinez, G. Wertheim, T. Kambayashi, J. Baur, D. Teachey, D. Fajgenbaum   +16 more
semanticscholar   +1 more source

Castleman Disease: An Unexpected Cause of a Solitary Pleural Mass

Case Reports in Radiology, 2013
Castleman disease (CD) is a rare benign lymphoproliferative disorder, the etiology of which is unclear. Clinically it may manifest as localized disease (unicentric) or disseminated disease (multicentric).
Fiachra Moloney, Maria Twomey, John Hinchion, Michael Maher   +3 more
doaj   +1 more source