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Observation of lymphadenopathy, systemic symptoms, and treatment in suspected indolent cutaneous B-cell lymphomas.
Puccio, Jordyn; Huang, Ying; Viveiros, Matthew D; Reneau, John C; Chung, Catherine; Spaccarelli, Natalie; Dulmage, Brittany.
Afiliación
  • Puccio J; Medical Student Research Program, The Ohio State University College of Medicine, Columbus, OH, USA.
  • Huang Y; Division of Hematology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Viveiros MD; Medical Student Research Program, The Ohio State University College of Medicine, Columbus, OH, USA.
  • Reneau JC; Division of Hematology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Chung C; Department of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Spaccarelli N; Division of Hematology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Dulmage B; Department of Pathology, The Ohio State University Wexner Medical Center, 540 Officenter Pl Suite 240, 43230, Columbus, OH, USA.
Arch Dermatol Res ; 316(5): 199, 2024 May 22.
Article en En | MEDLINE | ID: mdl-38775835
ABSTRACT

BACKGROUND:

Following the initial diagnosis of a marginal zone or follicle center lymphoma on skin biopsy, patients undergo staging to determine the extent of disease.

OBJECTIVE:

We sought to characterize the frequency that these patients were found to have a systemic nodal disease upon work-up as well as the impact of imaging on disease management.

METHODS:

We conducted a retrospective chart review of patients presenting with a working diagnosis of PCMZL or PCFCL treated at The Ohio State University from 1990 to 2022. Data collected included patient history, progress notes, virtual encounters, laboratory results, presentation features, imaging, and pathology. Biomarkers included ANA, SSA/SSB, BCL6 and H. Pylori labs, bone marrow biopsies, positive imaging, and need of systemic medication and mortality.

RESULTS:

71 patients with suspected PCMZL and PCFCL were identified. 66 of 71 patients underwent imaging. Of this group, 12 patients (9 with suspected PCFCL and 3 with suspected PCMZL) demonstrated lymphadenopathy on imaging. Of these 12 patients, 5 underwent biopsy of suspected lymph nodes, and 3 had biopsy-proven nodal involvement and received systemic therapy. Of the remaining 7 patients with evidence of lymphadenopathy on imaging, 4 were thought to have reactive lymph nodes, and 3 were treated empirically with systemic chemotherapy due to the extent or progression of their disease. Of patients with imaging negative for lymphadenopathy, 3 of 52 (5.8%) patients with received systemic treatment, while 49 of 52 patients (94.2%) received localized treatment.

LIMITATIONS:

Most of the relationships between this data were correlational and patients selected for this study were limited to a single institution.

CONCLUSION:

Prospective study of the role of imaging without subsequent lymph biopsy to direct treatment decisions is warranted.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Linfadenopatía Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Arch Dermatol Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Linfadenopatía Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Arch Dermatol Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos