1.Primary smooth muscle tumor in the male reproductive system: a report of 5 cases and review of the literature.
Hong-Yu ZHUANG ; Yong LUO ; Xue-Min XU ; Tao PENG ; Dong CHEN ; Fei TENG
National Journal of Andrology 2013;19(8):714-718
OBJECTIVETo systematically study the clinical diagnosis and treatment of smooth muscle tumor in the male reproductive system.
METHODSWe analyzed the ultrasonographic features, pathological findings, treatment strategies and postoperative follow-up results of 5 male patients with smooth muscle tumor in the reproductive system, and reviewed other relevant literature.
RESULTSCompared with leiomyoma, leiomyosarcoma exhibited stronger mixed echoes than the testis at ultrasonography, typical mitotic phase (> or = 2/10 HP) of tumor cells at HE staining, and significant expressions of HIF-1alpha and Glut-1 at immunohistochemistry. No relapse was observed in the 2 cases of leiomyoma during the 10-year follow-up after simple tumor resection, nor were recurrence and metastasis in another 3 cases of leiomyosarcoma during the first year after radical surgery without combined radio- and chemo-therapy.
CONCLUSIONPrimary smooth muscle tumor of the male reproductive system is difficult to be diagnosed. Ultrasonography can help to preliminarily screen leiomyosarcoma. For those with possible leiomyosarcoma, preoperative MRI and intraoperative frozen sectioning examinations are recommended for the possibility of lymphatic metastasis. Postoperative radiotherapy and chemotherapy should be chosen cautiously for those confirmed with leiomyosarcoma by pathological examination.
Adult ; Genital Neoplasms, Male ; diagnosis ; therapy ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Smooth Muscle Tumor ; diagnosis ; therapy
3.Construction of adenoviral vector encoding soluble human sTNFRI-IgGFc cDNA and its expression in human airway smooth muscle cells (HASMCs).
Jin SU ; Changxuan YOU ; Shaoxi CAI ; Li MA ; Xiaoning WANG ; Qian WEN ; Wei LUO ; Yongta HUANG
Chinese Journal of Biotechnology 2008;24(5):774-779
Tumour necrosis factor (TNF-a) is a pro-inflammatory cytokine that has been implicated in many aspects of the airway pathology in asthma, and which has recently been highlighted as potentially important in refractory asthma. To study the feasibility of local treatment of asthma with recombinant adenovirus vector carrying soluble extra-cellular region of TNF receptor I-IgGFc (sTNFRI-IgGFc) fusion protein, The sTNFRI-IgGFc gene was subcloned into the adenovirus shuttle plasmid pDC316, the products were co-transfected into HEK293 cell line with helper plasmid pBHGloxDeltaE1,3Cre. The recombinant adenovirus (Ad-sTNFRI-IgGFc) was produced by homologous recombination of above 2 plasmids in HEK293 cells. After identification with PCR, Ad-sTNFRI-IgGFc was amplified and purified, its titer was measured by TCID50 assay. The transcription and expression of sTNFRI-IgGFc gene in transfected human airway smooth muscle cells (HASMCs) was detected by RT-PCR, ELISA and immunological histochemistry. The anti-TNF activity assay of transfected HASMCs culture supernatant was measured by MTT. Ad-sTNFRI-IgGFc was successfully constructed with the titer of 3x10(10) TCID50/mL. Ad-sTNFRI-IgGFc can transfect HASMC with high efficacy. The transcription of sTNFRI-IgGFc mRNA and the expression of protein were confirmed in the transfected HASMCs. Moreover, the product in 100 microL expression supernatant could completely antagonize the cytolytic effect of 2ng TNFa on L929 cells, even at 1/64 dilution. This study forms the basement of the experiment study on local treatment of asthma with adenovirus expressing sTNFRI-IgGFc.
Adenoviridae
;
genetics
;
metabolism
;
Asthma
;
therapy
;
Bronchi
;
cytology
;
Cells, Cultured
;
Genetic Vectors
;
genetics
;
Humans
;
Immunoglobulin Fc Fragments
;
biosynthesis
;
genetics
;
Immunoglobulin G
;
biosynthesis
;
genetics
;
Myocytes, Smooth Muscle
;
cytology
;
metabolism
;
Receptors, Tumor Necrosis Factor
;
biosynthesis
;
genetics
;
Recombinant Fusion Proteins
;
biosynthesis
;
genetics
;
pharmacology
;
Transfection
;
Tumor Necrosis Factor-alpha
;
antagonists & inhibitors
4.Malignant Rhabdoid Tumor of the Cerebellum in an Adult: A case report.
Young Min KIM ; Jae Hee SUH ; Tae Sook KIM ; Shin Kwang KHANG
Korean Journal of Pathology 1998;32(6):460-465
Malignant rhabdoid tumor (MRT) is a rare and highly aggressive neoplasm of infancy and childhood. Although it was originally described and most frequently reported in the kidney, it may occur in various extra-renal sites such as the liver, thymus, and soft tissue. In the last decade primary central nervous system (CNS) MRTs have been reported in both the supra- and infratentorial compartments. Patients with CNS MRT were generally below the age of two and reports in adults are extremely rare. This is a case of primary cerebellar MRT in a 24-year-old woman, who had presented with intermittent headache, vocal cord palsy, and cerebellar dysfunctions such as abnormal finger to nose test and tandem gait. By magnetic resonance imaging scan, a well-enhancing solid mass was demonstrated at the posterior fossa filling the 4th ventricle, which extended into the medulla and cervical cord via the foramen of Magendie. Histologically, the monotonous polygonal tumor cells were arranged in diffuse sheet with occasional hemorrhagic necrosis. The nuclei were vesicular and eccentrically located due to eosinophilic, PAS-positive, intracytoplasmic inclusions with prominent nucleoli. They were diffusely or focally immunoreactive for vimentin, neurofilament, cytokeratin, GFAP, synaptophysin, and smooth muscle actin, while epithelial membrane antigen and desmin were negative. Ultrastructurally, the polyhedral tumor cells were densely packed with primitive intercellular junctions. Scanty fibrillar intermediate filaments were intermingled with cellular organelles. Postoperatively, craniospinal irradiation and systemic chemotherapy have been done and she has been free of tumor recurrence during the 13 months' follow-up periods.
Actins
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Adult*
;
Central Nervous System
;
Cerebellar Diseases
;
Cerebellum*
;
Craniospinal Irradiation
;
Desmin
;
Drug Therapy
;
Eosinophils
;
Female
;
Fingers
;
Follow-Up Studies
;
Gait
;
Headache
;
Humans
;
Intercellular Junctions
;
Intermediate Filaments
;
Keratins
;
Kidney
;
Liver
;
Magnetic Resonance Imaging
;
Mucin-1
;
Muscle, Smooth
;
Necrosis
;
Nose
;
Organelles
;
Recurrence
;
Rhabdoid Tumor*
;
Synaptophysin
;
Thymus Gland
;
Vimentin
;
Vocal Cord Paralysis
;
Young Adult