Primary ethmoidal lymphoma

D. B. Mendelsohn; Y. Hertzanu

doi:10.1016/S0009-9260(82)80388-7

Primary ethmoidal lymphoma

D. B. Mendelsohn
, Y. Hertzanu

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

Primary ethmoidal lymphoma is rare. The clinical and radiological findings are non-specific. Computed tomography (CT) is useful in delineating the extent of the tumour as well as for post-irradiation therapy follow-up. Three cases with the above condition are presented and one who was examined following radiotherapy had both clinical and radiographic evidence of regression of the lymphomatous lesion.

Original language	English
Pages (from-to)	631-633
Number of pages	3
Journal	Clinical Radiology
Volume	33
Issue number	6
DOIs	https://doi.org/10.1016/S0009-9260(82)80388-7
State	Published - 1 Jan 1982
Externally published	Yes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

ASJC Scopus subject areas

Radiology Nuclear Medicine and imaging

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10.1016/S0009-9260(82)80388-7

Cite this

@article{5cf8b95a53ab407e8fb7eb02d1fb4988,

title = "Primary ethmoidal lymphoma",

abstract = "Primary ethmoidal lymphoma is rare. The clinical and radiological findings are non-specific. Computed tomography (CT) is useful in delineating the extent of the tumour as well as for post-irradiation therapy follow-up. Three cases with the above condition are presented and one who was examined following radiotherapy had both clinical and radiographic evidence of regression of the lymphomatous lesion.",

author = "Mendelsohn, \{D. B.\} and Y. Hertzanu",

year = "1982",

month = jan,

day = "1",

doi = "10.1016/S0009-9260(82)80388-7",

language = "English",

volume = "33",

pages = "631--633",

journal = "Clinical Radiology",

issn = "0009-9260",

publisher = "W.B. Saunders Ltd",

number = "6",

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TY - JOUR

T1 - Primary ethmoidal lymphoma

AU - Mendelsohn, D. B.

AU - Hertzanu, Y.

PY - 1982/1/1

Y1 - 1982/1/1

N2 - Primary ethmoidal lymphoma is rare. The clinical and radiological findings are non-specific. Computed tomography (CT) is useful in delineating the extent of the tumour as well as for post-irradiation therapy follow-up. Three cases with the above condition are presented and one who was examined following radiotherapy had both clinical and radiographic evidence of regression of the lymphomatous lesion.

AB - Primary ethmoidal lymphoma is rare. The clinical and radiological findings are non-specific. Computed tomography (CT) is useful in delineating the extent of the tumour as well as for post-irradiation therapy follow-up. Three cases with the above condition are presented and one who was examined following radiotherapy had both clinical and radiographic evidence of regression of the lymphomatous lesion.

UR - https://www.scopus.com/pages/publications/0020453325

U2 - 10.1016/S0009-9260(82)80388-7

DO - 10.1016/S0009-9260(82)80388-7

M3 - Article

C2 - 7140145

AN - SCOPUS:0020453325

SN - 0009-9260

VL - 33

SP - 631

EP - 633

JO - Clinical Radiology

JF - Clinical Radiology

IS - 6

ER -

Primary ethmoidal lymphoma

Abstract

UN SDGs

ASJC Scopus subject areas

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