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testis chapter

Chapter Overview: Testis and Testicular Adnexa

  • Overview of key topics to be covered.

    • Normal embryology and anatomy of the testis.

    • Cryptorchidism (undescended testis).

    • Atrophy and infertility issues related to the testis.

    • Various non-neoplastic lesions.

    • Tumors of the testis.

    • Anatomy of testicular adnexa including rete testis, epididymis, and spermatic cord.

Normal Embryology and Anatomy of the Testis

  • Phases of Testicular Development:

    • Static Phase: Birth to age 4 years; tubules filled with undifferentiated cells.

    • Growth Phase: Ages 4 to 10 years; gradual growth of tubule and cell size.

    • Development Phase: Begins around age 10; onset of puberty marked by increase in gonadotropins and spermatozoa formation.

  • Structure of Adult Testis:

    • Average weight: 15–19 g (right testis typically heavier).

    • Capsule consists of three layers:

      • Outer serosa (tunica vaginalis).

      • Tunica albuginea.

      • Tunica vasculosa.

    • The mediastinum contains blood vessels, nerves, and portions of the rete testis.

    • Parenchyma divided into about 250 lobules; each lobule contains seminiferous tubules.

    • Histologic Components:

      • Sertoli cells (supporting germ cells).

      • Leydig cells (produce testosterone).

      • Germ cells at various development stages (spermatogonia, spermatocytes, spermatids, spermatozoa).

  • Spermatogenesis Timeline:

    • Process takes approximately 70 days, involves several maturation stages in an overlapping helical pattern.

    • Sertoli cells play crucial roles in nurturing germ cells and may express intermediate filaments (e.g., vimentin).

Cryptorchidism

  • Definition: Condition of undescended testes; more common in abdominal retention.

  • Incidence: Affects 1 in 10 males, with 1 in 100 remaining undescended permanently.

  • Management: If not correct by age 2-3, surgical intervention (orchidopexy) recommended to prevent anatomical changes.

  • Fertility Outcomes:

    • Unilateral cryptorchidism results in higher rates of fertility if corrected early.

    • Gross appearances in adulthood show atrophic changes in the tubules, often leading to infertility.

Atrophy and Infertility of the Testis

  • Causes of Testicular Atrophy:

    • Examples Include:

      • Cryptorchidism.

      • Orchitis, particularly mumps post-puberty.

      • Liver cirrhosis affecting estrogen levels.

      • Radiation and chemotherapy exposure.

    • Impact of Atrophy:

      • Histologically, testes may show varying conditions ranging from complete absence of germ cells (Sertoli cell-only syndrome) to areas of fibrosis and spermatogenic arrest.

  • Male Infertility Contributors:

    • Classified into three categories: pretesticular (hormonal issues), testicular (direct testicular disease), and post-testicular (obstruction).

  • Evaluation of Infertility:

    • Comprehensive assessment includes semen analysis, hormonal levels, and possible biopsy (especially in cases of azoospermia).

Non-Neoplastic Lesions and Conditions

  • Various histopathological issues affecting the testis:

    • Granulomatous Orchitis: Inflammation due to non-specific reactions, sometimes related to sperm degeneration.

    • Infarcts: Resulting from torsion or other vascular issues; can mimic neoplasms histologically.

    • Malakoplakia and Other Histiocytic Disorders: Various inflammatory conditions observed microscopically.

Tumors of the Testis

  • Classification: Major categories include:

    • Germ cell tumors (90% of testicular tumors).

    • Sex cord-stromal tumors.

    • Primary non-specific testicular tumors.

    • Metastatic tumors.

  • Epidemiology and Demographics:

    • Germ cell tumors are rare overall but predominant in young males (ages 25-29).

    • Increasing incidence, with factors such as cryptorchidism and genetic predispositions noted.

  • Clinical Presentation:

    • Often presents as a painless enlargement of the testis; may metastasize to lungs or retroperitoneum.

    • Bilaterality is rare but increased in undescended cases.

  • Molecular and Genetic Features:

    • Specific genetic abnormalities such as isochromosome 12p associated with invasive germ cell tumors.

    • Variability in genetic changes in different tumor types, influencing treatment and prognosis.