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An 8-Year-Old Boy With Fever, Splenomegaly, and Pancytopenia
Author(s) -
Rachel Offenbacher,
Brad Rybinski,
Tuhina Joseph,
Nora E. Rahmani,
Thomas Boucher,
Daniel A. Weiser
Publication year - 2020
Publication title -
pediatrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.611
H-Index - 345
eISSN - 1098-4275
pISSN - 0031-4005
DOI - 10.1542/peds.2019-2372
Subject(s) - medicine , pallor , pancytopenia , tachypnea , abdominal pain , pediatrics , abdominal distension , fever of unknown origin , hepatosplenomegaly , emergency department , physical examination , abdomen , lethargy , malignancy , surgery , disease , tachycardia , bone marrow , psychiatry
An 8-year-old boy with no significant past medical history presented to his pediatrician with 5 days of fever, diffuse abdominal pain, and pallor. The pediatrician referred the patient to the emergency department (ED), out of concern for possible malignancy. Initial vital signs indicated fever, tachypnea, and tachycardia. Physical examination was significant for marked abdominal distension, hepatosplenomegaly, and abdominal tenderness in the right upper and lower quadrants. Initial laboratory studies were notable for pancytopenia as well as an elevated erythrocyte sedimentation rate and C-reactive protein. Computed tomography (CT) of the abdomen and pelvis showed massive splenomegaly. The only significant history of travel was immigration from Albania 10 months before admission. The patient was admitted to a tertiary care children's hospital and was evaluated by hematology-oncology, infectious disease, genetics, and rheumatology subspecialty teams. Our multidisciplinary panel of experts will discuss the evaluation of pancytopenia with apparent multiorgan involvement and the diagnosis and appropriate management of a rare disease.

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