Page 729 - Textbook of Pathology, 6th Edition
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3. Teratoma with malignant transformation. This is an  Sertoli Cell Tumours (Androblastoma)             713
            extremely rare form of teratoma in which one or more of  Sertoli cell tumours correspond to arrhenoblastoma of the
            the tissue elements show malignant transformation. Such  ovary. They may occur at all ages but are more frequent in
            malignant change resembles morphologically with typical  infants and children. These tumours may elaborate oestrogen
            malignancies in other organs and tissues and commonly  or androgen and may account for gynaecomastia in an adult,
            includes rhabdomyosarcoma, squamous cell carcinoma  or precocious sexual development in a child.
            and adenocarcinoma.
                                                                 MORPHOLOGIC FEATURES. Grossly, the tumour is
           Mixed Germ Cell Tumours                               fairly large, firm, round, and well circumscribed. Cut
           About 60% of germ cell tumours have more than one of the  surface of the tumour is yellowish or yellow-grey.
           above histologic types (except spermatocytic seminoma) and  Microscopically,  Sertoli cell tumour is composed of
           are called mixed germ cell tumours. The clinical behaviour  benign Sertoli cells arranged in well-defined tubules.
           of these tumours is worsened by inclusion of more aggressive
           tumour component in a less malignant tumour. Interestingly,  Majority of Sertoli cell tumours are benign but about 10%
           metastases of the mixed germ cell tumours may not exactly  may metastasise to regional lymph nodes.
           reproduce the histologic types present in the primary
           tumour.                                             Granulosa Cell Tumour
              The most common combinations of mixed germ cell  This is an extremely rare tumour in the testis and resembles
           tumours are as under:                               morphologically with its ovarian counterpart (Chapter 24).
           1. Teratoma, embryonal carcinoma, yolk sac tumour and
           syncytiotrophoblast.                                MIXED GERM CELL-SEX CORD STROMAL TUMOURS
           2. Embryonal carcinoma and teratoma (teratocarcinoma).
           3. Seminoma and embryonal carcinoma.                An example of combination of both germ cells and sex cord
                                                               stromal components is gonadoblastoma.
           SEX CORD-STROMAL TUMOURS
                                                               Gonadoblastoma                                         CHAPTER 23
           Tumours arising from specialised gonadal stroma are classi-
           fied on the basis of histogenesis. The primitive mesenchyme  Dysgenetic gonads and undescended testis are predisposed
           which forms the specialised stroma of gonads in either sex  to develop such combined proliferations of germ cells and
           gives rise to theca, granulosa and lutein cells in the female,  sex cord-stromal elements. The patients are commonly
           and Sertoli and interstitial Leydig cells in the male. Since the  intersexuals, particularly phenotypic females. Most of the
           cell of origin of primitive mesenchyme is identical, Sertoli  gonadoblastomas secrete androgen and therefore produce
           and interstitial Leydig cell tumours may occur in the ovaries  virilisation in female phenotype. A few, however, secrete
           (in addition to theca cell, granulosa cell and lutein cell  oestrogen.
           tumours). Likewise, the latter three tumours may occur in
           the testis (in addition to Sertoli cell and Leydig cell tumours).  MORPHOLOGIC FEATURES. Grossly, the tumour is of
           All these tumours secrete various hormones. The biologic  variable size, yellowish-white and soft.
           behaviour of these tumours generally cannot be determined  Microscopically,  gonadoblastoma is composed of 2
           on histological grounds alone but is related to clinical  principal cell types—large germ cells resembling
           parameters and hormonal elaboration by these tumours.  seminoma cells, and small cells resembling immature
                                                                 Sertoli, Leydig and granulosa cells. Call-Exner bodies of
           Leydig (Interstitial) Cell  Tumour                    a granulosa cell tumour may be present.              The Male Reproductive System and Prostate
           Leydig cell tumours are quite uncommon. They may occur  Prognosis largely depends upon the malignant potential
           at any age but are more frequent in the age group of 20 to 50  of the type of germ cell components included.
           years. Characteristically, these cells secrete androgen, or both
           androgen and oestrogen, and rarely corticosteroids. Bilateral  OTHER TUMOURS
           tumours may occur typically in congenital adrenogenital
           syndrome.                                           Malignant Lymphoma
            MORPHOLOGIC FEATURES. Grossly, the tumour          Malignant lymphomas comprises 5% of testicular malignan-
            appears as a small, well-demarcated and lobulated  cies and is the most common testicular tumour in the elderly.
            nodule. Cut surface is homogeneously yellowish or  Bilaterality is seen in half the cases. Most common are large
            brown.                                             cell non-Hodgkin’s lymphoma of B cell type.
            Histologically, the tumour is composed of sheets and
            cords of normal-looking Leydig cells. These cells contain  Rare Tumours
            abundant eosinophilic cytoplasm and Reinke’s crystals
            and a small central nucleus.                       In addition to the testicular tumours described above, some
                                                               other uncommon tumours in this location include: plasma-
              Most of Leydig cell tumours are benign. Only about 10%  cytoma, leukaemic infiltration, carcinoid tumour,
           may invade and metastasise.                         haemangioma, primary sarcomas and metastatic tumours.
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