Primary diffuse large B-cell lymphoma of the parietal bone

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F21%3A43921522" target="_blank" >RIV/00216208:11120/21:43921522 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00064173:_____/21:N0000016

Výsledek na webu

<a href="https://doi.org/10.48095/cccsnn2021214" target="_blank" >https://doi.org/10.48095/cccsnn2021214</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.48095/cccsnn2021214" target="_blank" >10.48095/cccsnn2021214</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Primary diffuse large B-cell lymphoma of the parietal bone

Popis výsledku v původním jazyce

Primary bone lymphoma (PBL) is a rare disease that accounts for about 5% of all extranodal lymphomas, and the most common subtype is a non-Hodgkin diffuse large B-cell lymphoma (DLBCL) represent approximately 50-92% of PBLs [1]. Much more common plasma cell tumors are not included in this entity. The lesion may be in a single focus or disseminated, since polyostotic disease occurs in approximately 15-20% of patients. PBL should be distinguished from much more common secondary bone involvement in the case of nodal or other extranodal lymphoma, whereas these may be indistinguishable. The most frequent sites of PBL are the femur, spine, and pelvic bones. PBL of the skull is uncommon. Herein, we present a rare case of a female patient with primary DLBCL of the parietal bone. 70-year-old Caucasian woman presented with a palpable slightly painful induration on the calva. The lesion was found in a control PET scan performed due to breast carcinoma in the patient&apos;s history. The subtype of breast carcinoma was not known at the recent presentation. The patient underwent a right-sided mastectomy and combined adjuvant radiotherapy, hormonal therapy, and chemotherapy with doxorubicine and endoxan because of mammary carcinoma resected 14 years prior to recent presentation.

Název v anglickém jazyce

Primary diffuse large B-cell lymphoma of the parietal bone

Popis výsledku anglicky

Primary bone lymphoma (PBL) is a rare disease that accounts for about 5% of all extranodal lymphomas, and the most common subtype is a non-Hodgkin diffuse large B-cell lymphoma (DLBCL) represent approximately 50-92% of PBLs [1]. Much more common plasma cell tumors are not included in this entity. The lesion may be in a single focus or disseminated, since polyostotic disease occurs in approximately 15-20% of patients. PBL should be distinguished from much more common secondary bone involvement in the case of nodal or other extranodal lymphoma, whereas these may be indistinguishable. The most frequent sites of PBL are the femur, spine, and pelvic bones. PBL of the skull is uncommon. Herein, we present a rare case of a female patient with primary DLBCL of the parietal bone. 70-year-old Caucasian woman presented with a palpable slightly painful induration on the calva. The lesion was found in a control PET scan performed due to breast carcinoma in the patient&apos;s history. The subtype of breast carcinoma was not known at the recent presentation. The patient underwent a right-sided mastectomy and combined adjuvant radiotherapy, hormonal therapy, and chemotherapy with doxorubicine and endoxan because of mammary carcinoma resected 14 years prior to recent presentation.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30204 - Oncology

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2021

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Česká a slovenská neurologie a neurochirurgie

ISSN

1210-7859

e-ISSN

—

Svazek periodika

84

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

CZ - Česká republika

Počet stran výsledku

3

Strana od-do

214-216

Kód UT WoS článku

000694710200017

EID výsledku v databázi Scopus

2-s2.0-85107633793