Results 51 to 60 of about 1,367,795 (274)

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

Prenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell, Samantha Stover, Nora Gibson, Timothy Olson, James Connelly, Matthew Grace, Jennifer Andrews   +6 more
wiley   +1 more source

Rheumatic manifestations of lymphoproliferative disorders

, 2007
The association between musculoskeletal features and lymphoproliferative disorders as well as the association of rheumatic diseases with an increased risk of malignancies is well ...
Braun, J (15515330), Kiltz, U (15515345), Brandt, J (15515348), Zochling, J (15526052)   +3 more
core   +1 more source

Lymphoproliferative disorders affecting organs of the head and neck

, 2022
Introduction. Lymphomas are a heterogenic group of tumors of the lymphatic and hematopoietic systems, and in many cases tumor process develops in the area of the head and neck including skin and mucosa, orbit, nasal cavity and paranasal sinuses, oral ...
I. M. Gelfand, A. E. Raportinova, R. I. Azizyan, F. M. Abbasbeyli, M. B. Pak, A. A. Akhundov, K. D. Ilkaev, I. A. Zaderenko, A. V. Ignatova, M. V. Bolotin, Yu. V. Alymov, V. I. Sokorutov, A. F. Batsev, V. T. Tsiklauri, F. Sh. Kamolova, D. K. Stelmakh, P. A. Zeynalova   +16 more
core   +1 more source

Long‐Term Outcomes After Elective Splenectomy for Haematological Disease: A 27‐Year Single‐Centre Study

ANZ Journal of Surgery, EarlyView.
Splenectomy is a safe and effective treatment option in selected patients with haematological disease, despite declining referrals over the last 27 years in the era of targeted therapies. Outcomes are favourable when performed laparoscopically and long‐term follow‐up demonstrates sustained haematologic benefit in surviving patients.
Salil Dutt Barrett, Anthony Downhill, Douglas Greer, William Stevenson, Ian Kerridge, Chris Ward, Matthew Greenwood, Naomi Mackinlay, Luke Coyle, Thomas J. Hugh   +9 more
wiley   +1 more source

Lymphoproliferative disorders associated with hypereosinophilia.

, 2012
Hypereosinophilia, defined as peripheral blood eosinophil counts > 1,500/μL, may complicate the course of various lymphoproliferative disorders. Among these, Hodgkin lymphoma (HL) and certain peripheral T-cell lymphomas (PTCLs) derived from CD4 cells ...
Garaud, Soizic, de Leval, Laurence, Roufosse, Florence, Roufosse, F., Garaud, S., de Leval, L.   +5 more
core   +1 more source

How to Do a Laparoscopic Iliac Lymph Node Biopsy Under Indocyanine Green (ICG) Guidance

ANZ Journal of Surgery, EarlyView.
ABSTRACT Isolated abdominal lymphadenopathy can be difficult to diagnose when lesions are inaccessible to percutaneous biopsy. We describe a laparoscopic common iliac lymph node biopsy performed using indocyanine green (ICG) fluorescence guidance. A 67‐year‐old woman with bilateral lower limb oedema was found to have an FDG‐avid right common iliac ...
Hong Xiang Lee, Julian Soares, Zi Qin Ng
wiley   +1 more source

Genetic diversity of the KIR/HLA system and susceptibility to hepatitis C virus-related diseases.

PLoS ONE, 2015
BackgroundThe variability in the association of host innate immune response to Hepatitis C virus (HCV) infection requires ruling out the possible role of host KIR and HLA genotypes in HCV-related disorders: therefore, we therefore explored the ...
Valli De Re, Laura Caggiari, Mariangela De Zorzi, Ombretta Repetto, Anna Linda Zignego, Francesco Izzo, Maria Lina Tornesello, Franco Maria Buonaguro, Alessandra Mangia, Domenico Sansonno, Vito Racanelli, Salvatore De Vita, Pietro Pioltelli, Emanuela Vaccher, Massimiliano Berretta, Cesare Mazzaro, Massimo Libra, Andrea Gini, Antonella Zucchetto, Renato Cannizzaro, Paolo De Paoli   +20 more
doaj   +1 more source

Lymphoproliferative disorder due to sulphasalazine.

, 2009
We present the case of a 57-year-old man who had been on sulphasalazine for 20 years for seropositive non-erosive rheumatoid arthritis and developed a lymphoproliferative disorder, which resolved completely on cessation of sulphasalazine.
Dubey, Shirish, Adebajo, A O
core   +1 more source

Immunodeficiency-Associated Epstein-Barr Virus-Positive B-cell Lymphoproliferative Disorders

, 2023
Sources of immune deficiency and dysregulation (IDD) are being increasingly recognized and defined, as are IDD-related B-cell lymphoproliferative lesions and lymphomas occurring in these patients. In this review, basic biology of Epstein-Barr virus (EBV)
Jennifer Chapman, Chapman, Jennifer
core   +1 more source

Is retinal vein occlusion an underrecognized paraneoplastic sentinel of lymphoma? A systematic review and meta‐analysis of ocular–haematological interactions

Acta Ophthalmologica, EarlyView.
Abstract Topic This systematic review and meta‐analysis evaluated the association between retinal vein occlusion (RVO) and lymphoma across two complementary evidence components: a qualitative clinical synthesis of RVO occurring in patients with lymphoma and a quantitative synthesis of subsequent cancer outcomes in patients with RVO. For the qualitative
Kai‐Yang Chen, Hoi‐Chun Chan, Chi‐Ming Chan   +2 more
wiley   +1 more source