ABSTRACT
Testosterone is required for the development and maintenance of the male accessory sex organs and their normal function. And it was reported that castration affect cells in the adult male rat accessory sex glands by induction of programmed cell death (apoptosis). So, in this study, the authors made an experiment to evaluate the effect of testosterone in the maure male rat penis and accessory sex glands following castration. Also, we utilized actinomycin D, a potent inhibitor of messenger and ribosomal RNA synthesis, in the experiment herein to assess the significance of regression process in the glands. Following are the changes in the serum testosterone level, the weight of the penis, ventral prostate and seminal vesicles and apoptosis occurrence of the control (castration, castration normal saline) and experimental (castration AD25, castration AD50) group of mature rats. 1. After castration, the control group and the experimental group showed decreased level of serum testosterone. 2. In the both groups, the weight of the penis, ventral prostate and seminal vesicles decreased gradually. 3. Compared to the control group, the castration AD25 did not show the inhibition of castration induced regression of penis and ventral prostate. However, castration AD50 showed the inhibition. 4 In the H-E staining and ApoTag in situ staining, the ventral prostate showed the most prominent apoptosis occurrence followed by the seminal vesicles and penis. These results suggest that after castration of the mature rat, due to testosterone deficiency, the weight of penis, ventral prostate and seminal vesicles decreased with the occurrence of apoptosis. Also, actinomycin D 50 micrometer seems to delay the regression process.
Subject(s)
Adult , Animals , Humans , Male , Rats , Apoptosis , Castration , Cell Death , Dactinomycin , Genitalia , Penis , Prostate , RNA, Ribosomal , Seminal Vesicles , TestosteroneABSTRACT
The trichofolliculoma is a rare tumor of the hair follicle occuring most often on the head and neck. We have experienced a case of 24-year-old female who had a small, dome-shaped, tan brown firm nodule on the nose. Under the clinical impression of a granuloma, an excisional biopsy of the nodule was done. Microscopically the lesion was composed of a large central cystic hair follicle with many srhall but well differenciated secondary hair follicles branching from the wall. Well developed secondary hair follicles were often grouped and were surrounded by a prominent stroma.
Subject(s)
Female , Humans , BiopsyABSTRACT
Richer's syndrome is a development of a high grade malignant lymphoma in a patient with preexisting chronic 1ymphocytic leukemia, small lymphocytic lymphoma or Waldenstrom's macroglobulinemia. A rare case of Richer's syndrome arising in the spleen of a 35-year-old-man was studied by morphology, immunohistochemistry and gene rearrangement study. He has had weight loss and night sweat for last 6 months. Hepatosplenomegaly and abdominal lymphadenopathy were noted on CT scanning. Especially an ovoid radiolucent mass was found within the image of splenomegaly. Lymph nodes and liver biopsy, bone marrow aspiration and splenectomy were done. In the lymph nodes, liver and bone marrow, well differentiated small lymphocytic infiltrations were found but, in the spleen, pleomorphic, large cells with occasional multinucleated giant cells formed a nodular mass surrounded by diffuse, extensive infiltration of small well differentiated lymphocytes. The two distinctive areas in the spleen had positive staining for B-cell marker (HLA-DR and L26), negative staining for T-cell marker (UCLH1), and positive staining for IgM heavy chain and kappa light chain by immuohistochemical study. so this case was diagnosed as a diffuse large cell 1ymphoma transformed from small lymphocytic lymphoma. We made an another effort to clarify their clonality. Gene rearrangement method usingcomplementarity.determining region 3(CDR3) of immunoglobulin heavy chain (IgH) gene and T-cell receptor gamma (TCRgamma) gene by polymerase chain reaction (PCR) technique was done. The two lymphomas in the spleen demonstrated the same rearrangement pattern in both IgH and TCRgamma gene. We think these findings strongly suggest that the large cell lymphoma has the same clonality with that of the small lymphocytic lymphoma.
Subject(s)
Male , HumansABSTRACT
Strumal carcinoma of the ovary is rare tumor of germ cell origin characterized by intimate mixture of thyroid tissue and carcinoid. We report a strumal carcinoid tumor associated with ipsilateral follicular cyst and contralateral mature cystic teratoma of the ovary in a 47-year-old woman. Histologically it was composed largely of trabeculae partly of insular carcinoid and focally of individual thyroid follicles. Many cells in the carcinoid areas and even some follicular areas contained abundant argyrophile granules, and they also, in the corresponding areas, demonstrated thyroglobulin. Electron microscopic findings revealed abundant neurosecretory granules and colloid material in the same cell. We agree that this tumor is derived from hybrid showing thyroid and neuroendocrine differenciation.
Subject(s)
Female , Humans , CystsABSTRACT
Lymphoid tumors of the orbit are rare, and sometimes it is not possible either clinically or histologically to differentiate between lymphoid tumor and pseudolymphoma. Some authors assert that the degree of cytologic differentiation appears to be the single most important factor for determining the prognosis of patients with orbital lymphoid lesions. However, the cytomorphologic basis is not so helpful to diagnose and classify our case, which shows some discrepancy between pathological findings and clinical and radiological findings. At first we misdiagnosed our case as orbital malignant lymphoma on the basis of cytomorphology and immunohistochemical study. But no responce to local intensive radiotherapy and the follow up study of the patient suggest orbital pseudolymphoma.