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1.
Spine J ; 7(6): 720-7, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17936690

RESUMEN

BACKGROUND: Spinal neurenteric cysts are very rare lesions, especially after the second decade of life. They account for 0.3% to 0.5% of all spinal tumors and occur most commonly in ventral locations. The cysts are usually removed via a posterior approach. PURPOSE: To present the clinical and radiologic results of patients with spinal neurenteric cysts who were treated via anterior approach procedures. STUDY DESIGN: This report is composed of two cervical neurenteric cyst cases that are compared with published studies. METHODS: We present two patients, 41- and 39-year-old women, each with a cervical intradural neurenteric cyst. Both of these patients had apparent neck pain without neurological deficit. MRI revealed neurenteric cysts located at C7 and C7-T1 levels. After anterior corpectomy, the intradural cysts were removed, and then fusion was performed. RESULTS: The postoperative period went well. The follow-up cervical MRI studies were performed at 3, 6, and 18 months postoperatively, and there were no abnormalities found. CONCLUSIONS: This study has led to the conclusion that although neurenteric cysts are rare in adults, they can still be present with only persistent neck pain and without neurological deficits. This may lead to misdiagnosis. The importance of MRI is not controversial in the early diagnosis. An anterior approach may be considered the first preference for surgical technique in patients with ventrally located neurenteric cysts.


Asunto(s)
Vértebras Cervicales/patología , Vértebras Cervicales/cirugía , Defectos del Tubo Neural/patología , Defectos del Tubo Neural/cirugía , Adulto , Femenino , Humanos , Imagen por Resonancia Magnética
2.
Kulak Burun Bogaz Ihtis Derg ; 9(5): 376-9, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12471287

RESUMEN

Nasal natural killer T-cell lymphoma is a very aggressive and destructive disease with a poor prognosis. We hereby present two male patients in whom diagnostic problems and a mortal course were encountered. One patient (age 31 years) had progressive ulceration in the nasal area. Two biopsies that had been taken elsewhere were inconclusive. The other patient (age 40 years) was referred with a previous histopathologic diagnosis of squamous cell carcinoma. He complained of an unhealing wound in the hard palate. Biopsies were repeated in each case. Diagnosis was made by immunohistochemical examination. Both patients died shortly after the diagnosis. The importance of obtaining an adequate and deep biopsy sample and employing sophisticated immunohistochemical examination is emphasized for an accurate diagnosis.


Asunto(s)
Linfoma de Células T/diagnóstico , Neoplasias Nasales/diagnóstico , Neoplasias Palatinas/diagnóstico , Adulto , Quimioterapia Adyuvante , Diagnóstico Diferencial , Resultado Fatal , Humanos , Linfoma de Células T/diagnóstico por imagen , Linfoma de Células T/tratamiento farmacológico , Linfoma de Células T/patología , Linfoma de Células T/cirugía , Masculino , Neoplasias Nasales/diagnóstico por imagen , Neoplasias Nasales/patología , Neoplasias Nasales/radioterapia , Neoplasias Nasales/cirugía , Neoplasias Palatinas/diagnóstico por imagen , Neoplasias Palatinas/tratamiento farmacológico , Neoplasias Palatinas/patología , Neoplasias Palatinas/cirugía , Radioterapia Adyuvante , Tomografía Computarizada por Rayos X
3.
Case Rep Med ; 2012: 189170, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22851974

RESUMEN

Paratesticular mesotheliomas are very rare tumors. In this paper, we present the management of a 38-year-old male patient with paratesticular malignant mesothelioma who was initially misdiagnosed and treated as recurrent epididymitis. After the final pathology report defining paratesticular mesothelioma during scrotal exploration, he underwent radical orchiectomy and hemiscrotal excision as a complementary, secondary procedure. His metastatic workup did not show any dissemination. Therefore, he did not receive any adjuvant treatment and remained disease-free for more than 2 years.

4.
Case Rep Med ; 2012: 639629, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22611408

RESUMEN

Hereditary kidney cancer patients with bilateral multiple kidney tumors represent challenges in the era of rapidly growing minimal invasive treatment techniques. Birt-Hogg-Dubé Syndrome (BHDS) is an autosomal dominant genodermatosis characterized by a triad of benign skin tumors (fibrofolliculomas, trichodiscomas, acrochordons) together with an increased risk of developing malignant renal tumors and pulmonary disease such as pneumothoraces and multiple lung cysts. The morbidity and mortality of the affected patients is determined by the presence of the kidney tumors, which tend to be multifocal and bilateral, as observed in other hereditary kidney cancer syndromes like von Hippel-Lindau disease, familial leiomyomatosis, and hereditary papillary renal cell carcinoma. Herein, a patient with BHDS, presenting with synchronous bilateral multiple kidney tumors, is reported. The report describes the management of kidney tumors with two-stage open nephron-sparing surgery in which the nonvascular clamping technique was utilized.

5.
Fertil Steril ; 95(8): 2661-4.e1, 2011 Jun 30.
Artículo en Inglés | MEDLINE | ID: mdl-21300348

RESUMEN

Slow-freezing and vitrification methods of human ovarian tissue cryopreservation were compared in terms of primordial follicle count and in vitro antimüllerian hormone (AMH) and estradiol production. Compared with fresh and slow-frozen ovaries, vitrified ovaries contained statistically significantly fewer primordial follicles and produced statistically significantly less AMH in vitro. Estradiol production from slow-frozen and vitrified ovaries was similar but statistically significantly lower than from fresh cultured strips.


Asunto(s)
Hormona Antimülleriana/metabolismo , Criopreservación/métodos , Congelación , Folículo Ovárico/metabolismo , Ovario/metabolismo , Vitrificación , Adulto , Análisis de Varianza , Estradiol/metabolismo , Femenino , Humanos , Factores de Tiempo , Técnicas de Cultivo de Tejidos
9.
BMC Res Notes ; 1: 12, 2008 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-18710537

RESUMEN

BACKGROUND: The aim of this study was to compare the results of palpation-versus ultrasound-guided thyroid fine-needle aspiration (FNA) biopsies. FINDINGS: Clinical data, cytology and histopathology results were retrospectively analyzed on all patients who underwent thyroid FNA biopsy in our outpatient endocrinology clinic between January 1998 and April 2003. The same investigators performed all thyroid FNAs (ASC) and cytological evaluations (KP). Subjects in the ultrasound-guided group were older, otherwise there were no differences in baseline characteristics (gender, thyroid function, the frequency of multinodular goiter, nodule diameter and nodule location) between groups. Cytology results in nodules aspirated by palpation (n = 202) versus ultrasound guidance (n = 184) were as follows: malignant 2.0% versus 2.7% (p = 0.74), benign 69.8% versus 79.9% (p = 0.02), indeterminate 1.0% versus 4.9% (p = 0.02), inadequate 27.2% versus 12.5% (p < 0.01). Malignant results were compared with Fisher's exact test. Other cytology categories were compared with chi-square test. Eighteen patients from the palpation- and 23 from ultrasound-guided group underwent surgery. In the palpation-guided group, the sensitivity of FNA was 100%, specificity 94%, positive predictive value 67% and negative predictive value 100%. In the ultrasound-guided group, the sensitivity of FNA was 100%, specificity 80%, positive predictive value 73% and negative predictive value 100%. CONCLUSION: We demonstrate that ultrasound guidance for thyroid FNA significantly decreases inadequate for evaluation category. We also confirm the high sensitivity and specificity of thyroid FNA biopsy in the diagnosis of thyroid cancer. Where available, we recommend universal application of ultrasound guidance for thyroid FNA biopsy as a standard component of this diagnostic technique.

10.
J Hand Surg Am ; 30(5): 1083-6, 2005 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16182071

RESUMEN

The occurrence of chondromyxoid fibroma in the hand is rare. We report a case of chondromyxoid fibroma involving the whole fourth metacarpal that was treated by curettage and cancellous bone allograft.


Asunto(s)
Neoplasias Óseas/diagnóstico , Huesos del Metacarpo , Neoplasias de Tejido Conjuntivo/diagnóstico , Adulto , Neoplasias Óseas/cirugía , Trasplante Óseo , Legrado , Fibroma/diagnóstico , Fibroma/cirugía , Humanos , Masculino , Neoplasias de Tejido Conjuntivo/cirugía , Procedimientos Ortopédicos/métodos
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