Oshibki v diagnostike i terapii khronicheskikh limfoleǐkozov.

E. I. Iakhnina; I. A. Astsaturov; A. V. Pivnik; R. S. Samoǐlova; A. M. Kremenetskaia; A. I. Vorob'ev

Oshibki v diagnostike i terapii khronicheskikh limfoleǐkozov.

Translated title of the contribution: Errors in the diagnosis and therapy of chronic lympholeukemias

E. I. Iakhnina, I. A. Astsaturov, A. V. Pivnik, R. S. Samoǐlova, A. M. Kremenetskaia, A. I. Vorob'ev

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

Abstract

The analysis of 67 cases of benign, progressive, tumor CLL, lymph node lymphocytoma, CLL sarcoma transformation showed that the cases were misdiagnosed in 35.8% cases. The most common mistake (25.4%) was aggressive chemotherapy based on histological diagnosis of prolymphocytic, prolymphocytic-lymphoblastic lymphosarcoma without consideration of cytological and clinical evidence, tumor phenotype. The authors think valid to use the following criteria in diagnosis of lymphoproliferative diseases: histological findings, clinical manifestations and blood picture, tumor cell cytology, primary location and predominant dissemination of the tumor, immunophenotype, characteristic chromosomal disorders, response to treatment.

Translated title of the contribution	Errors in the diagnosis and therapy of chronic lympholeukemias
Original language	Russian
Pages (from-to)	45-49
Number of pages	5
Journal	Terapevticheskii Arkhiv
Volume	67
Issue number	7
State	Published - 1995

Cite this

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title = "Oshibki v diagnostike i terapii khronicheskikh limfoleǐkozov.",

abstract = "The analysis of 67 cases of benign, progressive, tumor CLL, lymph node lymphocytoma, CLL sarcoma transformation showed that the cases were misdiagnosed in 35.8% cases. The most common mistake (25.4%) was aggressive chemotherapy based on histological diagnosis of prolymphocytic, prolymphocytic-lymphoblastic lymphosarcoma without consideration of cytological and clinical evidence, tumor phenotype. The authors think valid to use the following criteria in diagnosis of lymphoproliferative diseases: histological findings, clinical manifestations and blood picture, tumor cell cytology, primary location and predominant dissemination of the tumor, immunophenotype, characteristic chromosomal disorders, response to treatment.",

author = "Iakhnina, {E. I.} and Astsaturov, {I. A.} and Pivnik, {A. V.} and Samoǐlova, {R. S.} and Kremenetskaia, {A. M.} and Vorob'ev, {A. I.}",

year = "1995",

language = "Russian",

volume = "67",

pages = "45--49",

journal = "Terapevticheskii Arkhiv",

issn = "0040-3660",

publisher = "Consilium MediCum",

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TY - JOUR

T1 - Oshibki v diagnostike i terapii khronicheskikh limfoleǐkozov.

AU - Iakhnina, E. I.

AU - Astsaturov, I. A.

AU - Pivnik, A. V.

AU - Samoǐlova, R. S.

AU - Kremenetskaia, A. M.

AU - Vorob'ev, A. I.

PY - 1995

Y1 - 1995

N2 - The analysis of 67 cases of benign, progressive, tumor CLL, lymph node lymphocytoma, CLL sarcoma transformation showed that the cases were misdiagnosed in 35.8% cases. The most common mistake (25.4%) was aggressive chemotherapy based on histological diagnosis of prolymphocytic, prolymphocytic-lymphoblastic lymphosarcoma without consideration of cytological and clinical evidence, tumor phenotype. The authors think valid to use the following criteria in diagnosis of lymphoproliferative diseases: histological findings, clinical manifestations and blood picture, tumor cell cytology, primary location and predominant dissemination of the tumor, immunophenotype, characteristic chromosomal disorders, response to treatment.

AB - The analysis of 67 cases of benign, progressive, tumor CLL, lymph node lymphocytoma, CLL sarcoma transformation showed that the cases were misdiagnosed in 35.8% cases. The most common mistake (25.4%) was aggressive chemotherapy based on histological diagnosis of prolymphocytic, prolymphocytic-lymphoblastic lymphosarcoma without consideration of cytological and clinical evidence, tumor phenotype. The authors think valid to use the following criteria in diagnosis of lymphoproliferative diseases: histological findings, clinical manifestations and blood picture, tumor cell cytology, primary location and predominant dissemination of the tumor, immunophenotype, characteristic chromosomal disorders, response to treatment.

UR - http://www.scopus.com/inward/record.url?scp=0029185866&partnerID=8YFLogxK

M3 - Article

SN - 0040-3660

VL - 67

SP - 45

EP - 49

JO - Terapevticheskii Arkhiv

JF - Terapevticheskii Arkhiv

IS - 7

ER -

Oshibki v diagnostike i terapii khronicheskikh limfoleǐkozov.

Abstract

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