B-Symptomatik bei unklarer mediastinaler Lymphadenopathie: Fallbericht eines 72-jährigen Patienten mit VEXAS-Syndrom

A. Ripke; A. Münchau; N. von Bubnoff; S. Jendrek; S. Kopelke; C. Kümpers; P. Parschke; S. Schinke; C. Khandanpour

doi:10.1007/s00108-023-01543-9

B-Symptomatik bei unklarer mediastinaler Lymphadenopathie: Fallbericht eines 72-jährigen Patienten mit VEXAS-Syndrom

A. Ripke^*, A. Münchau, N. von Bubnoff, S. Jendrek, S. Kopelke, C. Kümpers, P. Parschke, S. Schinke, C. Khandanpour

^*Korrespondierende/r Autor/-in für diese Arbeit

1 Zitat (Scopus)

Abstract

The case of a 72-year-old male patient who presented to our centre for rare diseases with recurrent fever, night sweats and weight loss with initially confirmed mediastinal lymphadenopathy is reported. Investigation of lymph node material was unrevealing. As an additional finding, the patient had a myelodysplastic syndrome. VEXAS syndrome (vacuoles, E1 enzyme, X‑linked, autoinflammatory, somatic) could be confirmed on the basis of a bone marrow biopsy and genetic testing.

Titel in Übersetzung	B symptoms in unexplained mediastinal lymphadenopathy: Case report of a 72-year-old male patient with VEXAS syndrome
Originalsprache	Deutsch
Zeitschrift	Innere Medizin (Germany)
Jahrgang	64
Ausgabenummer	8
Seiten (von - bis)	810-814
Seitenumfang	5
ISSN	2731-7080
DOIs	https://doi.org/10.1007/s00108-023-01543-9
Publikationsstatus	Veröffentlicht - 08.2023

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

Profilbereich: Lübeck Integrated Oncology Network (LION)
Zentren: Universitäres Cancer Center Schleswig-Holstein (UCCSH)

DFG-Fachsystematik

2.22-14 Hämatologie, Onkologie

Dokumente

10.1007/s00108-023-01543-9

Weitere Links

Link to publication in Scopus

Zitieren

@article{51f3bc9ad76e43749a596b502058f18f,

title = "B-Symptomatik bei unklarer mediastinaler Lymphadenopathie: Fallbericht eines 72-j{\"a}hrigen Patienten mit VEXAS-Syndrom",

abstract = "The case of a 72-year-old male patient who presented to our centre for rare diseases with recurrent fever, night sweats and weight loss with initially confirmed mediastinal lymphadenopathy is reported. Investigation of lymph node material was unrevealing. As an additional finding, the patient had a myelodysplastic syndrome. VEXAS syndrome (vacuoles, E1 enzyme, X‑linked, autoinflammatory, somatic) could be confirmed on the basis of a bone marrow biopsy and genetic testing.",

author = "A. Ripke and A. M{\"u}nchau and \{von Bubnoff\}, N. and S. Jendrek and S. Kopelke and C. K{\"u}mpers and P. Parschke and S. Schinke and C. Khandanpour",

note = "Publisher Copyright: {\textcopyright} 2023, The Author(s), under exclusive licence to Springer Medizin Verlag GmbH, ein Teil von Springer Nature.",

year = "2023",

month = aug,

doi = "10.1007/s00108-023-01543-9",

language = "Deutsch",

volume = "64",

pages = "810--814",

journal = "Innere Medizin (Germany)",

issn = "2731-7080",

publisher = "Springer Medizin",

number = "8",

}

TY - JOUR

T1 - B-Symptomatik bei unklarer mediastinaler Lymphadenopathie

T2 - Fallbericht eines 72-jährigen Patienten mit VEXAS-Syndrom

AU - Ripke, A.

AU - Münchau, A.

AU - von Bubnoff, N.

AU - Jendrek, S.

AU - Kopelke, S.

AU - Kümpers, C.

AU - Parschke, P.

AU - Schinke, S.

AU - Khandanpour, C.

PY - 2023/8

Y1 - 2023/8

N2 - The case of a 72-year-old male patient who presented to our centre for rare diseases with recurrent fever, night sweats and weight loss with initially confirmed mediastinal lymphadenopathy is reported. Investigation of lymph node material was unrevealing. As an additional finding, the patient had a myelodysplastic syndrome. VEXAS syndrome (vacuoles, E1 enzyme, X‑linked, autoinflammatory, somatic) could be confirmed on the basis of a bone marrow biopsy and genetic testing.

AB - The case of a 72-year-old male patient who presented to our centre for rare diseases with recurrent fever, night sweats and weight loss with initially confirmed mediastinal lymphadenopathy is reported. Investigation of lymph node material was unrevealing. As an additional finding, the patient had a myelodysplastic syndrome. VEXAS syndrome (vacuoles, E1 enzyme, X‑linked, autoinflammatory, somatic) could be confirmed on the basis of a bone marrow biopsy and genetic testing.

UR - https://www.scopus.com/pages/publications/85168339656

U2 - 10.1007/s00108-023-01543-9

DO - 10.1007/s00108-023-01543-9

M3 - Übersichtsarbeiten

AN - SCOPUS:85168339656

SN - 2731-7080

VL - 64

SP - 810

EP - 814

JO - Innere Medizin (Germany)

JF - Innere Medizin (Germany)

IS - 8

ER -

B-Symptomatik bei unklarer mediastinaler Lymphadenopathie: Fallbericht eines 72-jährigen Patienten mit VEXAS-Syndrom

Abstract

UN SDGs

Strategische Forschungsbereiche und Zentren

DFG-Fachsystematik

Dokumente

Weitere Links

Fingerprint

Zitieren