Angioimmunoblastic lymphadenopathy: Termination as diffuse lymphosarcoma with plasmacytoid features

A. O. Fayemi; M. Ali; E. V. Braun; T. DeCecio

Angioimmunoblastic lymphadenopathy: Termination as diffuse lymphosarcoma with plasmacytoid features

A. O. Fayemi, M. Ali, E. V. Braun, T. DeCecio

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

2 Scopus citations

Abstract

The evolution of angioimmunoblastic lymphadenopathy (AILD) to a malignant lymphoma with plasmacytic features in a 77-year-old woman is presented. The transition occurred within one month. Other previously reported cases of malignant transformation in AILD are reviewed. The high mortality rate and the diffuse organ involvement characteristically found in AILD would suggest that the disorder is neoplastic ab initio.

Original language	English
Pages (from-to)	39-43
Number of pages	5
Journal	Mount Sinai Journal of Medicine
Volume	46
Issue number	1
State	Published - 1979
Externally published	Yes

Cite this

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title = "Angioimmunoblastic lymphadenopathy: Termination as diffuse lymphosarcoma with plasmacytoid features",

abstract = "The evolution of angioimmunoblastic lymphadenopathy (AILD) to a malignant lymphoma with plasmacytic features in a 77-year-old woman is presented. The transition occurred within one month. Other previously reported cases of malignant transformation in AILD are reviewed. The high mortality rate and the diffuse organ involvement characteristically found in AILD would suggest that the disorder is neoplastic ab initio.",

author = "Fayemi, {A. O.} and M. Ali and Braun, {E. V.} and T. DeCecio",

year = "1979",

language = "English",

volume = "46",

pages = "39--43",

journal = "Mount Sinai Journal of Medicine",

issn = "0027-2507",

publisher = "Levy Library Press",

number = "1",

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TY - JOUR

T1 - Angioimmunoblastic lymphadenopathy

T2 - Termination as diffuse lymphosarcoma with plasmacytoid features

AU - Fayemi, A. O.

AU - Ali, M.

AU - Braun, E. V.

AU - DeCecio, T.

PY - 1979

Y1 - 1979

N2 - The evolution of angioimmunoblastic lymphadenopathy (AILD) to a malignant lymphoma with plasmacytic features in a 77-year-old woman is presented. The transition occurred within one month. Other previously reported cases of malignant transformation in AILD are reviewed. The high mortality rate and the diffuse organ involvement characteristically found in AILD would suggest that the disorder is neoplastic ab initio.

AB - The evolution of angioimmunoblastic lymphadenopathy (AILD) to a malignant lymphoma with plasmacytic features in a 77-year-old woman is presented. The transition occurred within one month. Other previously reported cases of malignant transformation in AILD are reviewed. The high mortality rate and the diffuse organ involvement characteristically found in AILD would suggest that the disorder is neoplastic ab initio.

UR - http://www.scopus.com/inward/record.url?scp=0018742807&partnerID=8YFLogxK

M3 - Article

C2 - 312425

AN - SCOPUS:0018742807

SN - 0027-2507

VL - 46

SP - 39

EP - 43

JO - Mount Sinai Journal of Medicine

JF - Mount Sinai Journal of Medicine

IS - 1

ER -

Angioimmunoblastic lymphadenopathy: Termination as diffuse lymphosarcoma with plasmacytoid features

Abstract

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