1.2 Cases of Prostatic Myosarcoma : Rhabdomyosarcoma andn Leiomyosarcoma.
Do Hoon YANG ; Tae Hoon LEE ; Dong Ik KIM ; Jung Min SIM ; Sung Joo HONG ; Min Sung LEE
Korean Journal of Urology 2000;41(11):1432-1436
No abstract available.
Leiomyosarcoma*
;
Myosarcoma*
;
Rhabdomyosarcoma*
2.Expressions and Diagnostic Usefulness of MIB-1 and p53 in Uterine Smooth Muscle Tumors.
Mi Jin KIM ; Yong Jin KIM ; Seung Ho LEESEUNGHO
Korean Journal of Pathology 2001;35(6):524-530
BACKGROUND: Controversy still remains concerning the criteria for the categorization of uterine smooth muscle tumors by conventional histologic examination. Various ancillary techniques have been used to improve diagnostic accuracy. METHODS: Immunohistochemical study of MIB-1 and p53 was performed on 10 usual leiomyomas (UL), 13 cellular leiomyomas (CL), 5 bizarre leiomyomas (BL), 2 cases of intravenous leiomyomatosis (IL), 5 smooth muscle tumors of uncertain malignant potential (STUMP) and 8 leiomyosarcomas (LMS), to investigate the diagnostic value of MIB-1 and p53 in uterine smooth muscle tumors. RESULTS: The MIB-1 labelling index was low in ULs and their variants (mean 5.67+/-5.53), but it was increased in STUMPs (17.67+/-6.51) and markedly increased in LMSs (35.71+/-11.35). In ULs and their variants, no immunostaining for p53 was noted except in one case of BL, while 2 (40%) of 5 STUMPs and 3 (38%) of 8 LMSs showed positive reactions for p53. There were significant differences among leiomyoma, STUMP and LMS in the MIB-1 labelling index and p53 expression. CONCLUSIONS:These results suggest that both abnormal expressions of p53 and a high MIB-1 labelling index are frequently associated with leiomyosarcoma. Our data also indicate that the classification system of Kempson and Hendrickson is well correlated with the MIB-1 labelling index.
Classification
;
Immunohistochemistry
;
Ki-67 Antigen
;
Leiomyoma
;
Leiomyomatosis
;
Leiomyosarcoma
;
Muscle, Smooth*
;
Smooth Muscle Tumor*
;
Uterine Neoplasms
3.Alveolar rhabdomyosarcoma of left testis: report of a case.
Chinese Journal of Pathology 2012;41(2):128-129
Adenocarcinoma
;
metabolism
;
pathology
;
Adult
;
Desmin
;
metabolism
;
Diagnosis, Differential
;
Humans
;
Lung Neoplasms
;
secondary
;
Lymphatic Metastasis
;
Male
;
Melanoma
;
metabolism
;
pathology
;
Rhabdomyosarcoma, Alveolar
;
metabolism
;
pathology
;
surgery
;
Sarcoma, Alveolar Soft Part
;
metabolism
;
pathology
;
Testicular Neoplasms
;
metabolism
;
pathology
;
surgery
;
Testis
;
metabolism
;
pathology
4.Granular Cell Myoblastoma of the Orbit: A Case Report.
Ye Cheol KIM ; Gook Ki KIM ; Bong Arm RHEE ; Yeung Keun LEE
Journal of Korean Neurosurgical Society 1978;7(1):207-212
Granular cell myoblastoma is a relatively uncommon lesion of debatable history appearing as a small, solitary but occasionally multiple neoplasm and usually benign course. Most granular cell myoblastoma have been observed tongue, skin and subcutaneous tissue and in the breast but only rarely in the orbit and we know of only 12 well-documented orbital myoblastoma at present. We have recently seen a orbital granuloma cell myoblastoma occurring in a 39 year-old woman, the tumor was firmly attached to the muscle cone and caused exophthalmos with exodeviation of the left eye and was totally removed from the transcranial-orbital unroofing procedure.
Adult
;
Breast
;
Exophthalmos
;
Exotropia
;
Female
;
Granular Cell Tumor*
;
Granuloma
;
Humans
;
Neoplasms, Muscle Tissue
;
Orbit*
;
Skin
;
Subcutaneous Tissue
;
Tongue
5.Alveolar Soft Part Sarcoma (Malignant Granular Cell Myoblastoma) in Axilla (Pectoral Muscle): Report of a Case
The Journal of the Korean Orthopaedic Association 1971;6(4):411-414
Since that first description of the so-called granular cell myoblastoma by Abrikossoff in 1926, it has been reported as occuring in many sites. This tumor is an unusual but not rare tumor. From the number of reviewed case reports(550) upto now, it appears that the occurence of multiple granular cell tumors (36) is much more common (7–16%) than traditionally believed. The precise histogenesis of this tumor is open to question. Most of this tumor is benign, but malignant ones have been reported. A case of malignant granular cell myoblastoma which was histologically proven and metastasized to the coracoid process of left scapula, the lung, and the skull, is presented with a brief of the literature.
Axilla
;
Granular Cell Tumor
;
Lung
;
Sarcoma, Alveolar Soft Part
;
Scapula
;
Skull
6.Imaging features of nonepithelial tumors of the bladder.
Chinese Journal of Oncology 2009;31(5):384-387
OBJECTIVETo summarize the imaging features of nonepithelial tumors of the bladder.
METHODSThe Imaging findings in 20 surgically treated patients with pathologically proved nonepithelial tumors of the bladder were retrospectively analyzed. The tumors included leiomyoma (n = 9), pheochromocytoma (n = 6), leiomyosarcoma (n = 2), rhabdomyosarcoma (n = 1), carcinosarcoma (n = 1), inflammatory myofibroblastoma (n = 1).
RESULTSThe leiomyomas were round or ellipse in shape with a sharp border and homogeneous density, and showed a low signal intensity on T1WI and T2WI in 1/1 case; slight enhancement on CT after contrast enhancement in 6/7 cases; and a poor blood supply on color Doppler ultrasonography in 3/4 cases. The pheochromocytoma had a round or oval shape and clear border, and slightly lobulated in 4/6 cases, homogeneous density/echo/signal in 5/6 cases, calcification in 1 case, low signal intensity on T1WI and high signal intensity on T2WI in 1/1 case, moderate or marked enhancement on CT and MRI in 4/5 cases, and strong blood supply on color Doppler ultrasonography in 3/4 cases. The inflammatory myofibroblastoma showed the same imaging features as the pheochromocytomas. Other malignant tumors showed an irregular configuration, with a poorly defined border, heterogeneous density/echo/signal and moderate to strong enhancement on CT.
CONCLUSIONMost leiomyomas and pheochromocytomas of the bladder show some typical imaging features on CT, MRI and ultrasound, which are helpful in making correct diagnosis and treatment plan preoperatively. Other malignant nonepithelial bladder tumors do not show special imaging characteristics and can only be diagnosed qualitatively.
Adult ; Aged ; Carcinosarcoma ; diagnosis ; diagnostic imaging ; Female ; Humans ; Leiomyoma ; diagnosis ; diagnostic imaging ; Leiomyosarcoma ; diagnosis ; diagnostic imaging ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Neoplasms, Muscle Tissue ; diagnosis ; diagnostic imaging ; Pheochromocytoma ; diagnosis ; diagnostic imaging ; Retrospective Studies ; Rhabdomyosarcoma ; diagnosis ; diagnostic imaging ; Tomography, X-Ray Computed ; Ultrasonography ; Urinary Bladder Neoplasms ; diagnosis ; diagnostic imaging
7.Uterine Leiomyomas with Perinodular Hydropic Degeneration: A Report of Two Cases.
Sung Nam KIM ; Jaejung JANG ; Kyu Rae KIM
Korean Journal of Pathology 2002;36(4):257-261
Hydropic degeneration is a frequent degenerative change in otherwise typical uterine leiomyomas. Very rarely, however, a significant amount of edema fluid accumulates around the fascicles of neoplastic smooth muscle bundles and forms the characteristic multinodular growth pattern that is called perinodular hydropic degeneration of leiomyoma (PHDL). The gross findings, showing a vague worm-like appearance and very rarely having an extrauterine extension, and the microscopic features, showing perinodular retraction artifacts forming pseudovascular spaces, make it difficult to differentiate the tumor from intravenous leiomyomatosis or myxoid leiomyosarcoma. We described two cases of leiomyomas showing perinodular hydropic degeneration (PHD), a condition that has rarely been described in English literature, and discussed the mechanism of forming "extrauterine extension" or cotyledonoid features. One of our cases showed the typical features of cotyledonoid dissecting leiomyoma, the other showed those of intramural dissecting leiomyoma. An awareness of the gross and microscopic findings of PHDL is important not to overdiagnose a benign smooth muscle neoplasm as a more aggressive type of tumor. It is thought that intramural dissecting leiomyoma, cotyledonoid dissecting leiomyoma, and PHDL are not distinct, but closely related subtypes showing different phases of evolutionary changes.
Artifacts
;
Edema
;
Leiomyoma*
;
Leiomyomatosis
;
Leiomyosarcoma
;
Muscle, Smooth
8.Embryonal Rhabdomyosarcoma of the Retroperitoneum in a Child: A Case Report.
Joon Sik LEE ; Mee Eun KIM ; Hae Wook PYUN ; Il Gee LEE ; Hy Jin KIM ; Jong Gil LEE ; Ik Su KIM
Journal of the Korean Radiological Society 2000;43(5):639-642
Rhabdomyosarcoma is the most common soft tissue sarcoma occurring in children, though retroperitoneal rhabdomyosarcoma is rare. We experienced a case of embryonal rhabdomyosarcoma of the retroperitoneum in a 43-month-old child, and describe the CT , MRI and pathologic findings.
Child*
;
Child, Preschool
;
Humans
;
Magnetic Resonance Imaging
;
Myosarcoma
;
Rhabdomyosarcoma
;
Rhabdomyosarcoma, Embryonal*
;
Sarcoma
9.Mesenchymal Cell Tumors of the Gastrointestinal Tract.
Keun Nam SHIN ; Young Kyu PARK ; Hae Hyeon SUH ; Young Bag KIM ; Dong Yee KIM ; Young Jin KIM
Journal of the Korean Surgical Society 1998;55(1):84-91
Mesenchymal cell tumors of the intestinal tract originate from connective tissues, muscles, fat, lymphatic tissues, blood vessels, and nerves in and beneath the submucosa. The most common site is the stomach, followed by the small bowel. Among the benign gastric neoplasms of mesodermal origin, those derived from smooth muscles constitute over 90%. Leiomyosarcomas of the stomach represent about 1% to 3% of primary malignant tumors and approximately 20% of submucosal tumors of the stomach. In the small bowel, leiomyoma is the most common benign tumor, and leiomyosarcoma represents about 19% of malignant tumors. The principle of surgical treatment of gastric mesenchymal tumors is local excision with a 2 to 3 cm margin in the surrounding gastric wall. We reviewed 48 cases of mesenchymal cell tumors of the gastrointestinal tract from January 1988 to March 1997 at the Department of Surgery, Namkwang General Hospital and Chonnam University Hospital School. The results are as follows : 1) There were 23 benign and 25 malignant tumors. 2) The most common benign tumor was leiomyoma (41.7%) and the most common malignant tumor was a leiomyosarcoma (47.9%). 3) The most common site was the stomach (52.1%), followed by the small bowel (25%); in the gastric tumor cases, the most common site was the body (60%). 4) The most common clinical manifestation was abdominal pain (37.5%), followed by bleeding (27.1%), a palpable mass, dyspepsia, and weight loss. 5) A wedge resection, a subtotal gastrectomy, or an enucleation of the mass was mainly performed on the stomach. Segmental resection and anastomosis was primarily performed in the small bowel. 6) Among the malignant tumors, a recurrence was noted in 8 patients(32%) : 7 leiomyosarcomas and 1 malignant histiocytoma. 7) The prognosis for a malignant leiomyosarcoma was better than that for an adenocarcinoma and was associated with tumor size and histologic grade (mitosis/10 HFP). However, we could not find any correlation between the prognosis and lymph node metastasis.
Abdominal Pain
;
Adenocarcinoma
;
Blood Vessels
;
Connective Tissue
;
Dyspepsia
;
Gastrectomy
;
Gastrointestinal Tract*
;
Hemorrhage
;
Histiocytoma
;
Hospitals, General
;
Humans
;
Intestines
;
Jeollanam-do
;
Leiomyoma
;
Leiomyosarcoma
;
Lymph Nodes
;
Lymphoid Tissue
;
Mesoderm
;
Muscle, Smooth
;
Muscles
;
Neoplasm Metastasis
;
Prognosis
;
Recurrence
;
Stomach
;
Stomach Neoplasms
;
Weight Loss