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1.
Hinyokika Kiyo ; 63(11): 471-474, 2017 Nov.
Article in Japanese | MEDLINE | ID: mdl-29232798

ABSTRACT

A 59-year-old woman was referred to our hospital with the finding of an incidentaloma in her right kidney. Computed tomographyand magnetic resonance imaging showed a solid tumor, approximately8 cm in diameter, at the lower pole of the right kidney. Partial nephrectomy was performed without a renal vessel clamp. Histopathologically, fibroblast-like spindle cells were proliferating with rich collagenous fibers, and tumor cells were infiltrated into the renal parenchyma. The tumor cells were stained positive with CD34, CD99, and bcl-2. The tumor was diagnosed as solitaryfibrous tumor originating from the kidney based on these histopathological findings. The patient was followed 3 years after surgery with neither recurrence nor metastasis.


Subject(s)
Kidney Neoplasms/diagnostic imaging , Kidney Neoplasms/pathology , Solitary Fibrous Tumors/diagnostic imaging , Female , Humans , Kidney Neoplasms/surgery , Magnetic Resonance Imaging , Middle Aged , Multimodal Imaging , Nephrectomy , Solitary Fibrous Tumors/surgery , Tomography, X-Ray Computed
2.
Hinyokika Kiyo ; 53(10): 733-5, 2007 Oct.
Article in Japanese | MEDLINE | ID: mdl-18018593

ABSTRACT

Proximal-type epithelioid sarcomas are rare soft tissue neoplasms occuring in the soma or thigh and often repeat recurrence and metastasis. We present a case of locally recurrenced proximal-type epithelioid sarcoma that could be treated by regional excision alone. A 62-year-old man visited our institute for a growing mass in the perineal region. Computed tomography (CT) showed a periurethral tumor 22 x 13 mm in diameter in the perineal region. The tumor was excised regionally, and the pathological examination with immunohistochemical staining revealed that the tumor was proximal-type epithelioid sarcoma. Local recurrence of the tumor occurred 2 years 7 months later without any metastatic lesion, and regional excision was performed again. Pathological diagnosis was proximal type epithelioid sarcoma and it was identical to the primary tumor. The patient is free of the disease 1 year after the second surgery of the tumor.


Subject(s)
Neoplasm Recurrence, Local , Sarcoma/surgery , Urethra/surgery , Urethral Neoplasms/surgery , Humans , Male , Middle Aged , Sarcoma/pathology , Treatment Outcome , Urethra/pathology , Urethral Neoplasms/pathology , Urologic Surgical Procedures, Male
3.
Hinyokika Kiyo ; 53(8): 551-5, 2007 Aug.
Article in Japanese | MEDLINE | ID: mdl-17874546

ABSTRACT

A 48-year-old man was referred to our institute for the evaluation of a concomitant gastric submucosal tumor and right adrenal tumor, incidentally found by ultrasound examination. Computed tomography showed a mass with a diameter of 6 cm adjacent to the stomach and the right adrenal tumor with a diameter of 3 cm. These tumors had similar characteristics in both plain and enhanced imagings. By magnetic resonance imaging, the intensity of the right adrenal tumor was equivalent to the liver in both T1 and T2 weighted images. On the other hand, the gastric submucosal tumor showed low intensity in T1 weighted images and high intensity in T2 weighted images. An adosterol scintigram showed slight accumulation at the region of adrenal tumor. The results of all conducted serum and urinary hormonal examinations were found to be within the normal range. Adrenalectomy and partial gastrectomy were performed laparoscopically. Pathological diagnosis of the adrenal tumor was a cortical adenoma, and that of the gastric submucosal tumor was gastrointestinal stromal tumor (GIST). The gastric tumor was immunohistochemically stained positive with the C-kit and CD34 and negative for s-100 protein and desmin. Histopathological diagnosis was coincident with gastric GIST and right adrenocortical adenoma, and the GIST was diagnosed as a high risk tumor because its diameter was over 5 cm.


Subject(s)
Adrenal Cortex Neoplasms/surgery , Adrenocortical Adenoma/surgery , Gastrointestinal Stromal Tumors/surgery , Laparoscopy , Stomach Neoplasms/surgery , Adrenal Cortex Neoplasms/complications , Adrenalectomy/methods , Adrenocortical Adenoma/complications , Gastrectomy/methods , Gastrointestinal Stromal Tumors/complications , Humans , Male , Middle Aged , Stomach Neoplasms/complications
4.
Urology ; 59(5): 692-7, 2002 May.
Article in English | MEDLINE | ID: mdl-11992842

ABSTRACT

OBJECTIVES: To determine the anatomic patterns of tumor distribution in radical prostatectomy specimens from nonpalpable prostate cancer. METHODS: Tumor maps directly traced from histologic slides of 62 radical prostatectomy specimens were superimposed by a computer-assisted imaging technique to create an idealized prostate gland at three levels: apex, mid-prostate, and base. To investigate specific patterns of tumor distribution, the sites of tumor in each quadrant were compared according to risk group stratification. The tumor extent was compared with the patterns of positivity in routine sextant biopsies. RESULTS: Among all patients, the tumor frequency was 85.5% in the mid-gland, 82.3% in the apex, and 48.4% in the base. Analysis by quadrant showed that tumors were significantly denser in the apex to mid-prostate. The primary extent of these tumors appeared to lie predominantly in the anterior half of the gland. Biopsy yields at the apex and mid-prostate appeared low compared with the frequency of cancers at these levels. No patterns specific to the different risk groups were found, but no tumors within the anterior base were found in the low-risk group. CONCLUSIONS: The primary extent of nonpalpable tumors appeared to lie predominantly in the anterior half of the gland at the apex to mid-prostate levels. Additional biopsy cores taken from more anterior regions of the gland may enhance the detection of nonpalpable cancers further.


Subject(s)
Image Processing, Computer-Assisted , Prostate/pathology , Prostatic Neoplasms/pathology , Aged , Biopsy , Humans , Male , Middle Aged , Neoplasm Staging , Prostatectomy , Risk Assessment
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