Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangement.


Journal

Virchows Archiv : an international journal of pathology
ISSN: 1432-2307
Titre abrégé: Virchows Arch
Pays: Germany
ID NLM: 9423843

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 25 05 2022
accepted: 21 07 2022
revised: 05 07 2022
pubmed: 26 7 2022
medline: 15 12 2022
entrez: 25 7 2022
Statut: ppublish

Résumé

Systemic anaplastic lymphoma kinase-negative (ALK-) anaplastic large cell lymphoma (ALCL) comprises a genomically heterogeneous disease that is considered a distinct entity by the 2016 World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues. Other than lymph nodes, systemic ALK- ALCL may affect extranodal tissues, sites where the inflammatory background may be especially prominent. In this scenario, myxoid change is exceptional in systemic ALK- ALCL. We describe a rare case of systemic ALK- ALCL with distinctive myxoid changes, carrying specific chromosomal aberrations that affect the clinical outcome. Careful morphological, immunohistochemical, and molecular workup is mandatory because a myxoid background should not be a reason to ignore the possibility of a lymphoma. Finally, extensive correlation with staging and the detection of prognostic biomarkers such as DUSP22 and TP63 rearrangements are essential for the diagnosis and prediction of clinical outcome in ALK- ALCL.

Identifiants

pubmed: 35879438
doi: 10.1007/s00428-022-03386-5
pii: 10.1007/s00428-022-03386-5
doi:

Substances chimiques

DUSP22 protein, human EC 3.1.3.48
Dual-Specificity Phosphatases EC 3.1.3.48
Mitogen-Activated Protein Kinase Phosphatases EC 3.1.3.16

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

975-979

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Stefano Fratoni (S)

Diagnostic Surgical Pathology Department/Hematopathology Section, Saint'Eugenio Hospital, Rome, Italy.

Malgorzata Monika Trawinska (MM)

Hematology Unit, Saint'Eugenio Hospital, piazzale dell'Umanesimo 10 (00144), Rome, Italy.

Anna Capalbo (A)

Medical Genetics Division, IRCCS Casa Sollievo Della Sofferenza Foundation, San Giovanni Rotondo, Foggia, Italy.

Laura Bernardini (L)

Medical Genetics Division, IRCCS Casa Sollievo Della Sofferenza Foundation, San Giovanni Rotondo, Foggia, Italy.

Maria Fabbretti (M)

Medical Genetics Division, IRCCS Casa Sollievo Della Sofferenza Foundation, San Giovanni Rotondo, Foggia, Italy.

Maurizio Martini (M)

Department of Human & Childhood Pathology "G. Barresi", University of Messina School of Medicine, Messina, Italy.

Pasquale Niscola (P)

Hematology Unit, Saint'Eugenio Hospital, piazzale dell'Umanesimo 10 (00144), Rome, Italy. pniscola@gmail.com.

Xiangfeng Frank Zhao (XF)

Department of Pathology, University of Arizona College of Medicine & Pathology & Laboratory Medicine Service, Phoenix VA Health Care System, Phoenix, AZ, USA.

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