Epitrochlear lymphadenopathy

Article information

Korean J Intern Med. 2019;34(6):1396-1396
Publication date (electronic) : 2018 December 6
doi : https://doi.org/10.3904/kjim.2018.218
Department of Internal Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India
Correspondence to Savita Kumari, M.D. Tel: +91-9914209674 E-mail: pgimerim1@gmail.com
Received 2018 June 20; Revised 2018 June 21; Accepted 2018 July 1.

A 62-year-old man with diffuse large B cell lymphoma presented with upper abdominal mass and shortness of breath. General physical examination revealed bilateral cervical, axillary, epitrochlear (Fig. 1), and inguinal lymphadenopathy. These nodes were symmetrical, large, discrete, firm, mobile, and nontender. A computed tomographic scan of the chest and abdomen showed gross left sided pleural effusion and a large lobulated lymph nodal mass in the retroperitoneum. He was started on chemotherapy using rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP).

Figure 1.

(A) Right epitrochlear lymphadenopathy (arrows). (B) Left epitrochlear lymphadenopathy (arrows).

Enlargement of epitrochlear nodes is almost always pathological and usually occurs with disorders causing generalized lymphadenopathy; such as non-Hodgkin’s lymphoma, chronic lymphocytic leukemia, human immunodeficiency virus infection, Epstein-Barr virus infection, sarcoidosis, or rarely, syphilis. It provides a useful discriminatory sign in the diagnosis of fever with lymphadenopathy.

Written informed consents were obtained.

Notes

No potential conflict of interest relevant to this article was reported.

Article information Continued

Figure 1.

(A) Right epitrochlear lymphadenopathy (arrows). (B) Left epitrochlear lymphadenopathy (arrows).