testicular neoplasm

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    TESTICULAR NEOPLASM

    Most important cause of firm, painless enlargement of the testis.

    5/100 000 males.

    20-34 yrs old.

    95% arise from germ cells.

    Cause- unknown.

    Cryptorchidism a/w 3-5x increase of risk of cancer. (10% of thecancer case)

    Intersex syndrome increase risk.

    More common in white.

    MORPHOLOGY

    Seminomas

    (Classic seminomas)

    Large, soft, well-demarcated, usually homogeneous,gray-white

    tumour

    Microscopically:

    Large + uniform cells distanct cell borders clear, glycogen-rich cytoplasm round nuclei with conspicuous nucleoliSpermatocytic seminomas

    A mixture of medium-sized cells, large uninucleate or

    multinucleate tumour cells, and small cells with round nuclei

    Embyronal carcinomas

    Ill-defined, invasive masses The constituent cells are large and primitive looking, with

    basophilic cytoplasm, indistinct cell borders, and large

    nuclei with prominent nucleoli

    Yolk sac tumours

    Often large and may be well demarcated Low cuboidal to columnar epithelial cells forming

    microcyst, sheets, glands, and papillae, often associated

    with eosinophilic hyaline globules

    Schiller-Duvall bodiesChoriocarcinomas

    Small, nonpalpable lesions Sheets of small cuboidal cells irregularly intermingled with

    or capped by large, eosinophilic syncytial cells

    Teratomas

    Masses that on cut surface often contain cysts andrecognizable areas of cartilage

    Mature teratomas- fully differentiated tissues Immature teratomas- immature somatic elementsMixed germ cell tumours

    40% of all testicular germ cell neoplasms Combinations of the any of the described patterns Most common-combination of teratoma, embryonal

    carcinoma, and yolk sac tumours

    Classification testicular germ cell tumors:

    Tumours w 1 histologic pattern

    Seminoma

    Non-seminomatous

    Embryonal carcinoma Yolk sac tumour Choriocarcinoma Teratomas

    Mature Immature With malignant transformation ofsomatic elements

    Tumours w multiple histologic pattern

    CLINICAL FEATURES

    Seminomas Non-seminomatous germ cell

    noeplasm

    Often remain confinedto the testis for

    prolonged intervals

    Metastases- iliac +para-aortic lymph

    nodes (upper lumbar

    region)

    Hematogenous spreadoccur later

    Metastasize ealier :

    haematogenous + lymphatic

    (lung +liver)

    Painless enlargement of testis

    STAGING

    Stage I: tumour confined to the testis

    Stage II: regional lymph node metastases only

    Stage III: nonregional lymph node and/or distant organ metastases

    SPECIAL FEATURES

    Assay of tumour markers:- secreted by tumor cell

    - important for clinical evaluation + staging

    hCG- produced by: synthiotropoblastic- always in choriocarcinoma + seminoma (xde

    cytotropoblastic)

    AFP:- is a glycoprotein synthesized by fetal yolk sac

    -indicate for the present of nonseminomatous

    - bcoz yolk sac x found in pure seminomas

    TREATMENT

    Chemotherapy

    Tx determine by:

    -Histologic pattern

    -The stage of disease at the time of diagnosis

    Seminoma:

    -radiosensitive

    -respond well to chemotherapy

    Non seminomatous tumour:

    -platinum-based chemotherapy regimens.

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