Journal article
Eruption of lymphocyte recovery with atypical lymphocytes mimicking a primary cutaneous T-cell lymphoma: a series of 12 patients.
-
Hurabielle C
Department of Dermatology, Hôpital Henri-Mondor, AP-HP, 94220 Créteil, France.
-
Sbidian E
Department of Dermatology, Hôpital Henri-Mondor, AP-HP, 94220 Créteil, France.
-
Beltraminelli H
Department of Dermatology, Inselspital Bern University Hospital, University of Bern, 3010 Bern, Switzerland.
-
Bouchindhomme B
Department of Pathology, Lille University Hospital, 59000 Lille, France.
-
Chassagne-Clément C
Department of Pathology, Centre Léon Bérard, 69008 Lyon, France.
-
Balme B
Department of Pathology, Lyon-Sud University Hospital, 69310 Pierre-Bénite, France.
-
Bossard C
Department of Pathology, Nantes University Hospital, 44093 Nantes Cedex 1, France.
-
Delfau-Larue MH
Department of Biological Hematology and INSERM U955 team 9, AP-HP, Henri-Mondor Hospital, 94220 Créteil, France.
-
Wolkenstein P
Department of Dermatology, Hôpital Henri-Mondor, AP-HP, 94220 Créteil, France.
-
Chosidow O
Department of Dermatology, Hôpital Henri-Mondor, AP-HP, 94220 Créteil, France.
-
Cordonnier C
Department of Hematology, AP-HP, Henri-Mondor Hospital, 94220 Créteil, France.
-
Toma A
Department of Hematology, AP-HP, Henri-Mondor Hospital, 94220 Créteil, France.
-
Pautas C
Department of Hematology, AP-HP, Henri-Mondor Hospital, 94220 Créteil, France.
-
Ortonne N
Department of Pathology and INSERM U955 team 9, AP-HP, Henri-Mondor Hospital, 94220 Créteil, France. Electronic address: nicolas.ortonne@aphp.fr.
Show more…
English
Eruption of lymphocyte recovery (ELR) may occur during bone marrow aplasia after chemotherapies. We reviewed the clinical and pathologic features of 12 patients (male-female ratio, 7:5; median age, 61 years) with an atypical ELR histologically mimicking a primary cutaneous T-cell lymphoma such as Sézary syndrome or CD30+ T-cell lymphoproliferative disorder. All the patients displayed an erythematous maculopapular eruption on the trunk and the limbs associated with fever. All but one had received a polychemotherapy for an acute myeloid leukemia (n=10) or a urothelial carcinoma (n=1) before the occurrence of the skin eruption. One had an autoimmune lymphoproliferative syndrome causing chronic agranulocytosis requiring granulocyte colony-stimulating factor injection. In all patients, the skin eruption was associated with a slight increase of white blood cell count followed by bone marrow recovery within the next weeks. All skin biopsies showed a dermal perivascular lymphocytic infiltrate containing atypical medium- to large-sized CD3+, CD4+ and CD8+, CD25+, ICOS+, PD1- lymphocytes with a strong CD30 expression in most instances (n=10), suggesting the recruitment of strongly activated T cells in the skin. In 6 patients, a diagnosis of CD30+ lymphoproliferative disorder or Sézary syndrome was proposed or suspected histopathologically, and only the clinical context allowed the diagnosis of ELR with a peculiar presentation with atypical lymphocytes. We describe a series of patients with an unusual form of ELR characterized by the presence of atypical activated T cells in the skin. On a practical ground, pathologists should be aware of this distinctive and misleading presentation.
-
Language
-
-
Open access status
-
closed
-
Identifiers
-
-
Persistent URL
-
https://sonar.ch/global/documents/178037
Statistics
Document views: 28
File downloads: