Scholarlink

Background <p>Syphilis is a re-emerging sexually transmitted infection known for its heterogeneous clinical manifestations and ability to mimic neoplastic, inflammatory, and infectious diseases. Testicular involvement is rare and may radiologically resemble testicular cancer, frequently leading to unnecessary orchiectomy. We report a case of syphilitic orchitis initially suspected to be a testicular malignancy, highlighting the importance of including syphilis in the differential diagnosis of atypical testicular lesions.</p> Case presentation <p>A previously healthy 36-year-old man presented with a two-day history of dull right testicular pain associated with a palpable lump and a faint skin rash present for approximately two weeks. Ultrasound and contrast-enhanced ultrasound identified a 9–12&#xa0;mm hypoechoic hypovascular intratesticular lesion suspicious for malignancy. Computed tomography showed no metastatic lesions, and serum tumor markers (LDH, HCG, AFP) were within normal ranges. A right orchifunicolectomy was performed. Histopathological examination revealed dense interstitial inflammatory infiltrates rich in plasma cells and lymphocytes without evidence of neoplasia. Immunohistochemical staining demonstrated numerous <i>Treponema pallidum</i> spirochetes within the lesion and epididymis, establishing the diagnosis of syphilitic orchitis. Serologic tests confirmed syphilis infection (TPHA positive; VDRL 1:128). Screening test for human immunodeficiency virus and other sexually transmitted infections was negative. Based on pathological findings and the concomitant skin rash, secondary syphilis with testicular involvement was diagnosed. The patient was treated with intramuscular benzathine penicillin G, achieving complete serologic response, with no recurrence after two years of follow-up.</p> Conclusions <p>Syphilitic orchitis is an uncommon but clinically relevant differential diagnosis of testicular masses. In the context of increasing syphilis incidence, particularly among high-risk populations, clinicians should consider serologic screening for <i>Treponema pallidum</i> in patients with atypical testicular lesions and negative tumor markers. Early recognition may support a conservative management approach, preventing unnecessary surgical procedures and ensuring prompt treatment.</p> Clinical trial number <p>Not applicable.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

A challenging diagnosis of syphilis in a patient with a testicular lump: a case report

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年7月17日

查看全文
  • Francesca Pennati,
  • Elisabetta Pedruzzi,
  • Paolo Botti,
  • Carla Scolari,
  • Paola Zanotti,
  • Maurizio Gulletta,
  • Laert Zeneli,
  • Deborha Pezzola,
  • Alberto Matteelli

摘要

Background

Syphilis is a re-emerging sexually transmitted infection known for its heterogeneous clinical manifestations and ability to mimic neoplastic, inflammatory, and infectious diseases. Testicular involvement is rare and may radiologically resemble testicular cancer, frequently leading to unnecessary orchiectomy. We report a case of syphilitic orchitis initially suspected to be a testicular malignancy, highlighting the importance of including syphilis in the differential diagnosis of atypical testicular lesions.

Case presentation

A previously healthy 36-year-old man presented with a two-day history of dull right testicular pain associated with a palpable lump and a faint skin rash present for approximately two weeks. Ultrasound and contrast-enhanced ultrasound identified a 9–12 mm hypoechoic hypovascular intratesticular lesion suspicious for malignancy. Computed tomography showed no metastatic lesions, and serum tumor markers (LDH, HCG, AFP) were within normal ranges. A right orchifunicolectomy was performed. Histopathological examination revealed dense interstitial inflammatory infiltrates rich in plasma cells and lymphocytes without evidence of neoplasia. Immunohistochemical staining demonstrated numerous Treponema pallidum spirochetes within the lesion and epididymis, establishing the diagnosis of syphilitic orchitis. Serologic tests confirmed syphilis infection (TPHA positive; VDRL 1:128). Screening test for human immunodeficiency virus and other sexually transmitted infections was negative. Based on pathological findings and the concomitant skin rash, secondary syphilis with testicular involvement was diagnosed. The patient was treated with intramuscular benzathine penicillin G, achieving complete serologic response, with no recurrence after two years of follow-up.

Conclusions

Syphilitic orchitis is an uncommon but clinically relevant differential diagnosis of testicular masses. In the context of increasing syphilis incidence, particularly among high-risk populations, clinicians should consider serologic screening for Treponema pallidum in patients with atypical testicular lesions and negative tumor markers. Early recognition may support a conservative management approach, preventing unnecessary surgical procedures and ensuring prompt treatment.

Clinical trial number

Not applicable.