A.I. BURNASYAN FMBC CLINICAL BULLETIN

ISSN 2782-6430 (print)

State Research Center −Burnasyan Federal Medical Biophysical
Center of Federal Medical Biological Agency

The journal is published in Russian.
Format – A4.
The periodicity of the journal is 4 times a year.

Issue №2 2025 год

A.I. Burnasyan  FMBC clinical bulletin. 2024 № 1

E.A. Praskurnichiy1,2, K.M. Badykova1, Ju.S. Kitaeva1, O.N. Lotkova2

Hodgkin’s Lymphoma and Klinefelter Syndrome: a Description of the Clinical Case

1International Office, State Research Center – Burnasyan Federal Medical Biophysical Center of Federal Medical Biological Agency, Moscow, Russiа

2Pirogov Russian National Research Medical University, Moscow, Russia

Contact person: Badykova Kseniya Mikhaylovna: badykova.gem@gmail.com

Abstract
Klinefelter syndrome is the most common chromosomal abnormality among others and is manifested mainly by hypogonadism, gynecomastia, and infertility. Against the background of KS, oncological diseases can develop, more often nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) due to genetic reparations, as well as osteoporosis as a result of androgen deficiency.
This article describes a clinical case of a patient with Klinefelter syndrome and the onset of Hodgkin’s lymphoma (HL) in order to assess the risk of osteopenia/osteoporosis in this patient. A patient with previously diagnosed KS went to the doctor complaining of weakness, fatigue, weight loss, local enlargement of the inguinal lymph nodes. The patient was diagnosed with NLPHL and standard pathogenetic therapy was performed. Taking into account the presence of risk factors for osteoporosis (the presence of Klinefelter syndrome, HL, chemotherapy), the patient underwent two-energy densitometry in the lumbar spine, neck and proximal femur in order to assess the condition of bone tissue. As a result, a decrease in bone mineral density was found in all measurement areas.
This clinical case describes a rather rare combination of three significantly different nosologies. Interestingly, two of them, namely HL and Klinefelter syndrome, contribute to the development of the third through various mechanisms. The presence of a decrease in bone density in this patient necessitates prevention. Despite the rare occurrence of such combined pathologies, the issue of timely diagnosis and prevention of complications from the musculoskeletal system in this category of patients remains relevant today

Keywords: Hodgkin’s lymphoma, Klinefelter syndrome, osteoporosis, bone mineral density, polychemotherapy

For citation: Praskurnichy EA, Badykova KM, Kitaeva YuS, Lotkova ON. Hodgkin’s Lymphoma and Klinefelter Syndrome: a Description of the Clinical Case. A.I. Burnasyan Federal Medical Biophysical Center Clinical Bulletin. 2024.1:18-21. (In Russian) DOI: 10.33266/2782-6430-2024-1-18-21

 

REFERENCES

  1. Voroncova M.V. Kalinchenko N.Ju. Sindrom Klajnfel’tera: obzor literatury po ispol’zovaniju sovremennyh metodov vspomogatel’nyh reproduktivnyh tehnologij // Problemy jendokrinologii. – 2020. – №66(6). – p. 31-38.
  2. Kalinchenko S.Ju., Vinogradov I.V. Sindrom Klajnfel’tera: klinika, diagnostika, lechenie // Farmateka. – 2008. – №17. – p. 70-75.
  3. Manusharova R.A., Cherkezova Je.I. Gipogonadizm u muzhchin // Medicinskij sovet. – 2012. – №5. – p. 40-47.
  4. Hasle H., Mellemgaard A., Nielsen J., Hansen J. Cancer incidence in men with Klinefelter syndrome // British Journal of Cancer. – 1995. – №71(2). – p. 416-420.
  5. Bonouvrie K., Bosch J., Akker M. Klinefelter syndrome and germ cell tumors: review of the literature // International Journal of Pediatric Endocrinology. – 2020. – №18
  6. Salieva S.S., Boranbaeva R.Z., Zhumadullaev B.M. Klinicheskij sluchaj mediastinal’noj teratomy u podrostka s sindromom Klajnfel’tera // Voprosy gematologii/onkologii i immunopatologii v pediatrii. – 2020. – №19(4). – p. 143-149.
  7. Rojas A., Vo D., Mwangi L. Oncologic manifestations of Klinefelter syndrome // Hormones (Athens). – 2020. – №19(4). – p. 497-504.
  8. Schatorjé E., Flier M., Seppänen M. Primary immunodeficiency associated with chromosomal aberration – an ESID survey // Orphanet Journal of Rare Diseases. – 2016. – №11(1)
  9. Mjakova N.V., Maschan A.A., Rumjancev A.G. Federal’nye klinicheskie rekomendacii po diagnostike i lecheniju limfomy Hodzhkina (limfogranulematoz) // Rossijskij zhurnal detskoj gematologii i onkologii. – 2015. – №4. – p. 79-90.
  10. Horowitz M., Wishart J, O’Loughlin P Osteoporosis and Klinefelter’s syndrome // Clinical endocrinology. – 1992. – №36(1). – С. 113-118.
  11. Humphreys M., Lavery P., Morris C., Nevin N. Klinefelter syndrome and non-Hodgkin lymphoma // Cancer Genetics and Cytogenetics. – 1997. – №97(2). – p. 111-113.
  12. Kitaeva Ju.S, Praskurnichij E.A. Prediktory snizhenija mineral’noj plotnosti kostnoj tkani u pacientov s limfomoj Hodzhkina, associirovannye s patogeneticheskoj terapiej // Arhiv vnutrennej mediciny. – 2023. – №13(1). – p. 36-45.

 

Conflict of interest. The authors declare no conflict of interest. 
Financing. The study had no sponsorship.
Contribution. Article was prepared with equal participation of the authors.
Article received: 29.02.2024. Accepted for publication: 14.03.2024

Scroll to Top