Primary spinal marginal zone lymphoma

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Primary spinal marginal zone lymphoma : case report and review of the literature. / Ahmadi, Sebastian A; Frank, Stephan; Hänggi, Daniel; Eicker, Sven O.

In: NEUROSURGERY, Vol. 71, No. 2, 08.2012, p. E495-508; discussion E508.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Ahmadi, SA, Frank, S, Hänggi, D & Eicker, SO 2012, 'Primary spinal marginal zone lymphoma: case report and review of the literature', NEUROSURGERY, vol. 71, no. 2, pp. E495-508; discussion E508. https://doi.org/10.1227/NEU.0b013e31824e50fb

APA

Ahmadi, S. A., Frank, S., Hänggi, D., & Eicker, S. O. (2012). Primary spinal marginal zone lymphoma: case report and review of the literature. NEUROSURGERY, 71(2), E495-508; discussion E508. https://doi.org/10.1227/NEU.0b013e31824e50fb

Vancouver

Bibtex

@article{deb7d117d27a452697ee53b8c2d10814,
title = "Primary spinal marginal zone lymphoma: case report and review of the literature",
abstract = "BACKGROUND AND IMPORTANCE: Marginal zone lymphoma (MZL) describes a heterogeneous group of indolent B-cell lymphomas. The World Health Organization recognizes 3 types of MZLs: splenic MZL, nodal MZL, and extranodal MZL of mucosa-associated lymphoid tissue. There is no consensus on the optimal adjuvant treatment modalities for intracranial primary MZLs. To date, no case of spinal primary MZL has been reported.CLINICAL PRESENTATION: We present the first case of spinal MZL diagnosed in a 65-year-old man with progressive paraparesis. He underwent surgical removal of the main spinal tumor mass, which extended epidurally from vertebral body T3 to T7. Surgery was followed by 10 sessions of local irradiation for a total dose of 31 Gy. On long-term follow-up in 2010, the patient was in good health without any signs of residual or recurrent disease. Twenty-seven publications reporting on 61 cases of intracranial primary MZL were identified and reviewed. In the majority of cases of marginal zone B-cell lymphoma, adjuvant radiotherapy was used, with some combining radiotherapy and chemotherapy after surgical removal of the bulk of the main tumor. Long-term follow-up in most patients showed no evidence of disease and clinical well-being years after the initial diagnosis.CONCLUSION: Chemotherapy and/or radiation have been used in larger case series. Although there is no defined treatment guideline for this rare disease entity, our review of the literature suggests a favorable prognosis when combining surgical and adjuvant radiotherapy approaches.",
keywords = "Aged, Decompression, Surgical, Humans, Lymphoma, B-Cell, Marginal Zone, Magnetic Resonance Imaging, Male, Spinal Cord Compression, Spinal Neoplasms, Thoracic Vertebrae, Treatment Outcome",
author = "Ahmadi, {Sebastian A} and Stephan Frank and Daniel H{\"a}nggi and Eicker, {Sven O}",
year = "2012",
month = aug,
doi = "10.1227/NEU.0b013e31824e50fb",
language = "English",
volume = "71",
pages = "E495--508; discussion E508",
journal = "NEUROSURGERY",
issn = "0148-396X",
publisher = "Lippincott Williams and Wilkins",
number = "2",

}

RIS

TY - JOUR

T1 - Primary spinal marginal zone lymphoma

T2 - case report and review of the literature

AU - Ahmadi, Sebastian A

AU - Frank, Stephan

AU - Hänggi, Daniel

AU - Eicker, Sven O

PY - 2012/8

Y1 - 2012/8

N2 - BACKGROUND AND IMPORTANCE: Marginal zone lymphoma (MZL) describes a heterogeneous group of indolent B-cell lymphomas. The World Health Organization recognizes 3 types of MZLs: splenic MZL, nodal MZL, and extranodal MZL of mucosa-associated lymphoid tissue. There is no consensus on the optimal adjuvant treatment modalities for intracranial primary MZLs. To date, no case of spinal primary MZL has been reported.CLINICAL PRESENTATION: We present the first case of spinal MZL diagnosed in a 65-year-old man with progressive paraparesis. He underwent surgical removal of the main spinal tumor mass, which extended epidurally from vertebral body T3 to T7. Surgery was followed by 10 sessions of local irradiation for a total dose of 31 Gy. On long-term follow-up in 2010, the patient was in good health without any signs of residual or recurrent disease. Twenty-seven publications reporting on 61 cases of intracranial primary MZL were identified and reviewed. In the majority of cases of marginal zone B-cell lymphoma, adjuvant radiotherapy was used, with some combining radiotherapy and chemotherapy after surgical removal of the bulk of the main tumor. Long-term follow-up in most patients showed no evidence of disease and clinical well-being years after the initial diagnosis.CONCLUSION: Chemotherapy and/or radiation have been used in larger case series. Although there is no defined treatment guideline for this rare disease entity, our review of the literature suggests a favorable prognosis when combining surgical and adjuvant radiotherapy approaches.

AB - BACKGROUND AND IMPORTANCE: Marginal zone lymphoma (MZL) describes a heterogeneous group of indolent B-cell lymphomas. The World Health Organization recognizes 3 types of MZLs: splenic MZL, nodal MZL, and extranodal MZL of mucosa-associated lymphoid tissue. There is no consensus on the optimal adjuvant treatment modalities for intracranial primary MZLs. To date, no case of spinal primary MZL has been reported.CLINICAL PRESENTATION: We present the first case of spinal MZL diagnosed in a 65-year-old man with progressive paraparesis. He underwent surgical removal of the main spinal tumor mass, which extended epidurally from vertebral body T3 to T7. Surgery was followed by 10 sessions of local irradiation for a total dose of 31 Gy. On long-term follow-up in 2010, the patient was in good health without any signs of residual or recurrent disease. Twenty-seven publications reporting on 61 cases of intracranial primary MZL were identified and reviewed. In the majority of cases of marginal zone B-cell lymphoma, adjuvant radiotherapy was used, with some combining radiotherapy and chemotherapy after surgical removal of the bulk of the main tumor. Long-term follow-up in most patients showed no evidence of disease and clinical well-being years after the initial diagnosis.CONCLUSION: Chemotherapy and/or radiation have been used in larger case series. Although there is no defined treatment guideline for this rare disease entity, our review of the literature suggests a favorable prognosis when combining surgical and adjuvant radiotherapy approaches.

KW - Aged

KW - Decompression, Surgical

KW - Humans

KW - Lymphoma, B-Cell, Marginal Zone

KW - Magnetic Resonance Imaging

KW - Male

KW - Spinal Cord Compression

KW - Spinal Neoplasms

KW - Thoracic Vertebrae

KW - Treatment Outcome

U2 - 10.1227/NEU.0b013e31824e50fb

DO - 10.1227/NEU.0b013e31824e50fb

M3 - SCORING: Journal article

C2 - 22314752

VL - 71

SP - E495-508; discussion E508

JO - NEUROSURGERY

JF - NEUROSURGERY

SN - 0148-396X

IS - 2

ER -