نتایج جستجو برای: lymphoproliferative lesion

تعداد نتایج: 103000  

2015
Sarah E. Halula Daniel G. Leino Manish N. Patel John M. Racadio Matthew P. Lungren

Posttransplant lymphoproliferative disorder (PTLD) is a well-described complication of solid organ and bone marrow transplants. The most common presentation is intra-abdominal lymphadenopathy or single or multiple intraparenchymal masses involving the liver, spleen, or kidneys. Here we describe the imaging and pathology findings of an unusual case of PTLD appearing as an intramuscular forearm l...

2017
Stéphanie Olivier Claire Dachelet Ivan Theate Isabelle Tromme Marie Baeck

CD30+ cutaneous anaplastic large-cell lymphoma is part of the CD30+ T-cell lymphoproliferative disorders. This type of lymphoma is in most cases indolent, with a high survival rate. We report the case of a 59-year-old patient with a 1-month lasting crusty lesion of the upper eyelid. Eyelid involvement is very uncommon, as the most frequent locations are the trunk and the limbs.

2012
Ji Hyun Kwon Soo Kee Min Mi Kyung Shin Yong Seong Lee Young-Goo Lee Young Hyeh Ko

Castleman disease is a rare lymphoproliferative lesion that is predominantly found in the mediastinum. Retroperitoneal and pararenal localizations are very rare. We describe a 36-year-old man with a hyaline vascular type of Castleman disease involving renal parenchyma and a paraaortic lymph node. Most reported renal Castleman disease was plasma cell type with systemic symptoms. Herein, we repor...

2011
Jason R. Andrews Yoon Andrew Cho-Park Judith Ferry Jeremy S. Abramson Gregory K. Robbins

Since its discovery in 1994, Kaposi's sarcoma-associated herpesvirus (KSHV) has been associated with lymphoproliferative disorders, particularly in patients infected with human immunodeficiency virus (HIV). The disorders most strongly linked to KSHV are multicentric Castleman's Disease (MCD), primary effusion lymphoma, and diffuse large B-cell lymphomas. We report an unusual case of KSHV-associ...

Journal: :iranian red crescent medical journal 0
bita geramizadeh department of pathology, shiraz university of medical sciences, iran +98-711-6474331, [email protected]; department of pathology, shiraz university of medical sciences, iran +98-711-6474331, [email protected] sama nikeghbalian department of hepatobiliary surgery, transplant research center, shiraz university of medical sciences, iran seyed mohsen dehghani department of pediatrics, shiraz university of medical sciences, iran ali bahador department of pediatric surgery, transplant research center, shiraz university of medical sciences, iran heshmatollah salahi department of surgery, transplant research center, shiraz university of medical sciences, iran

post-transplant lymphoproliferative disorder is a lymphocyte proliferating disease, usually of b cell origin, and rarely of t cell. involvement of liver itself in liver transplant recipients as the primary organ is not common. herein we report our experience in two patients who primarily presented in the allografted liver, both of whom were promptly diagnosed after liver biopsy and treated succ...

Journal: :acta medica iranica 0
mohammad ali mohagheghi department of surgical oncology, cancer institute, imam khomeini hospital center, tehran university of medical sciences, tehran, iran. ramesh omranipur department of surgical oncology, cancer institute, imam khomeini hospital center, tehran university of medical sciences, tehran, iran. fereshteh ensani department of pathology, cancer institute, imam khomeini hospital center, tehran university of medical sciences, tehran, iran. alireza ghannadan department of pathology, cancer institute, imam khomeini hospital center, tehran university of medical sciences, tehran, iran. shahriar shahriaran department of radiology, cancer institute, imam khomeini hospital center, tehran university of medical sciences, tehran, iran. farhad samiee radiation oncology, cancer institute, imam khomeini hospital center, tehran university of medical sciences, tehran, iran.

we present here a 32-year-old male with advanced lately diagnosed, right sided retroperitoneal mass, which had been already treated due to progressive muco-cutaneous lesions clinically consistent with psoriasis, during recent four years. the advanced retroperitoneal mass resected surgically and reported as hyaline-vascular castleman disease with a dense focus of coarse calcification, on histopa...

Journal: :Animal : an international journal of animal bioscience 2012
A Ferrari F S Weill M L Paz E M Cela D H González Maglio J Leoni

Since they were first described in 1993, it was found that recombinant variable fragments (rVHHs) of heavy-chain antibodies (HCAbs) from Camelidae have unusual biophysical properties, as well as a special ability to interact with epitopes that are cryptic for conventional Abs. It has been assumed that in vivo raised polyclonal HCAbs (pHCAbs) should behave in a similar manner than rVHHs; however...

2014
Etsuko Fujii Atsuhiko Kato Yu Jau Chen Koichi Matsubara Yasuyuki Ohnishi Masami Suzuki

Human tumor tissue line models established in the severely immunodeficient NOD.Cg-Prkdc(scid) Il2rg(tm1Sug)/Jic (NOD/Shi-scid, IL-2Rγ(null) or NOG) mouse are important tools for oncology research. During the establishment process, a lymphoproliferative lesion (LPL) that replaces the original tumor cells in the site of transplantation occurs. In the present study, we studied the impact of the LP...

Journal: :The British journal of ophthalmology 1983
A Garner A H Rahi J E Wright

A prospective immunological study of patients with proptosis due to intraorbital lesions composed largely or exclusively of lymphoid tissue indicates that the use of antisera to specific heavy and light chain antibody components can be helpful in distinguishing between polyclonal and truly neoplastic monoclonal disorders. On the basis of combined histological and immunological information it is...

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