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Spontaneous improvement in a pediatric patient with peripheral T‐cell lymphoma
Author(s) -
Kobayashi Ryoji,
Suzuki Daisuke,
Hori Daiki,
Kishimoto Kenji,
Sano Hirozumi,
Nakazawa Atsuko,
Yasuda Kazue,
Kobayashi Kunihiko
Publication year - 2015
Publication title -
pediatrics international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.49
H-Index - 63
eISSN - 1442-200X
pISSN - 1328-8067
DOI - 10.1111/ped.12784
Subject(s) - medicine , lymphoma , pancytopenia , peripheral t cell lymphoma , histopathology , lymph node biopsy , gastroenterology , pathology , bone marrow , t cell , immunology , immune system
Peripheral T‐cell lymphoma (PTCL) is rare in children, and it has a poor prognosis compared with other types of lymphoma. We report the case of a 7‐year‐old boy with spontaneous improvement of PTCL complicated by hemophagocytic syndrome as the initial symptom. He complained of pain and swelling of the right neck and presented with high fever. Pancytopenia, liver dysfunction, elevated ferritin and soluble interleukin 2 receptor were noted on laboratory tests. Peripheral blood plasma and white blood cells were positive for Epstein–Barr virus (EBV) genome but, after several days, the fever abated and laboratory data improved. On histopathology of lymph node biopsy, he was diagnosed as having PTCL not otherwise specified (PTCL‐NOS) with EBV infection. He received no chemotherapy and was disease free at the last follow up, 6 years 8 months after onset. This is probably the first case of spontaneous improvement in PTCL‐NOS. Careful treatment planning is therefore necessary in PTCL‐NOS, given the possibility of spontaneous improvement of symptoms.