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Autor:
Megan K. Dishop, Christiana Smith, Carrye R. Cost, Michael Wang, Edwin J. Asturias, Cathy Lee-Miller
Publikováno v:
The Journal of pediatrics. 165(6)
Multicentric Castleman disease (MCD) is a rare lymphoproliferative disorder that usually manifests with nonspecific symptoms, including fever and lymphadenopathy. Treatment of pediatric MCD varies greatly. A 21-month-old child was diagnosed with MCD
Autor:
Nedim Hadzic, Giorgina Mieli-Vergani, Ruth M Ayling, Edward R. Howard, Charles R. Buchanan, Mark Davenport, Russell Metcalfe
Publikováno v:
The Journal of Pediatrics. 138:932-935
We report on 7 patients referred for treatment of hepatic hemangioendothelioma with increased thyrotropin levels. The serum thyroxine level was decreased in 4 and increased in 2. Immunohistochemistry showed positive staining of tumor, but not of norm
Autor:
Brigitta U. Mueller, Barry D. Anderson, Maureen Farley, David Venzon, Shizuko Sei, John L. Sullivan, Douglas J. Schwartzentruber, Philip A. Pizzo, Katherine Luzuriaga, Gareth Tudor-Williams, Cecil H. Fox
Publikováno v:
The Journal of Pediatrics. 129:410-418
BACKGROUND: Lymph nodes serve as reservoirs for the replication of human immunodeficiency virus (HIV) type 1. Comparison of serial measurements of virus burden in lymph nodes and peripheral blood after a change in antiretroviral therapy may provide i
Publikováno v:
The Journal of pediatrics. 156(5)
To investigate whether renal vasculitis is the sole cause or merely a contributing cause of renal inflammation in Kawasaki disease (KD).This prospective study in a university medical center in Taiwan enrolled 24 children with KD between June 2004 and
Publikováno v:
The Journal of Pediatrics. 125:406-408
We compared pancreatic acinar and ductal secretion in two patients with Johanson-Blizzard syndrome, age-matched control subjects, and patients with other primary pancreatic diseases. Patients with Johanson-Blizzard syndrome had preservation of ductul
Autor:
Vas Novelli, Denis O’Hara, Anita E. Smyth, Emmanuelle Jouanguy, Jon Pritchard, Sid Dempsey, Rosie Hague, J. David M. Edgar, Allister J. Taggart, Louise Sweeney, Dinakantha S. Kumararatne, David A. Lammas, Jean-Laurent Casanova
Publikováno v:
The Journal of pediatrics. 139(4)
Two patients who were initially given a diagnosis of Langerhans' cell histiocytosis on the basis of the clinical, radiologic, and biopsy findings had mycobacterial infection subsequently identified. The correct diagnosis of dominant partial interfero
Publikováno v:
The Journal of pediatrics. 85(2)
Two infants with the hemolytic uremic syndrome are presented. Immunofluorescences studies were done on renal biopsies of each patient as well as on autopsy tissue of one of the patients who subsequently died. In contrast to previously reported immuno