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1.
Medicine (Baltimore) ; 97(48): e13406, 2018 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-30508941

RESUMEN

RATIONALE: Paraovarian cysts (PCs) are cystic tumors that can be encountered between the ovarian hilum and the ovarian fimbria located within the mesosalpinx and broad ligament, being usually diagnosed within the 3rd and 4th decade of life. PATIENT CONCERNS: We report the case of a 15-year-old female admitted in our clinic for consciousness loss, who was incidentally diagnosed with a giant pelvic cystic at ultrasound. DIAGNOSES: The magnetic resonance image showed a cystic mass of 170/140/85 mm, suggesting an origin from the left ovary, reaching the subhepatic area. INTERVENTIONS AND OUTCOMES: The surgical intervention revealed 3 PCs, a giant one and 2 smaller ones within the large ligament. The cysts were removed by laparoscopic approach, and the histologic examination did not reveal any signs of neoplasia. LESSONS: In addition to their rarity, giant PCs can be an incidental diagnosis in patients presenting unrelated symptoms resulting in increased difficulties related to the diagnosis. Moreover, the imagistic tools might not establish precisely the origin of these cysts, and therefore, the final diagnosis and treatment approach could be determined sometimes only during the surgical intervention.


Asunto(s)
Quiste Paraovárico/diagnóstico por imagen , Enfermedades de los Anexos , Adolescente , Ligamento Ancho , Femenino , Humanos , Hallazgos Incidentales , Laparoscopía/métodos , Imagen por Resonancia Magnética , Masculino , Quiste Paraovárico/patología , Quiste Paraovárico/cirugía , Ultrasonografía
2.
Rom J Morphol Embryol ; 57(4): 1415-1419, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-28174813

RESUMEN

Fetal ultrasonography remains the main diagnostic tool for the assessment of different malformation. Fetal limb anomalies can be either isolated, either associated with other malformations in context of different syndromes. We present two cases of isolated fetal limb anomalies involving the distal part of the upper limb, namely the fetal hand consisting in phalangeal aplasia detected through routine ultrasound fetal examination. We could not identify the etiology in any of the cases, but in one of them, we discovered a bilateral thumb anomaly of the mother's hand. Both fetuses were aborted spontaneously without any relation to the detected anomaly. The upper limb anomaly was confirmed by the clinical, radiological and anatomopathological examinations of the aborted fetuses. The early detection of fetal limb anomalies provides the opportunity of choosing the best therapeutic management. Genetic counseling must also be taken under consideration for further pregnancies.


Asunto(s)
Feto/patología , Deformidades Congénitas de la Mano/diagnóstico por imagen , Adulto , Femenino , Deformidades Congénitas de la Mano/patología , Humanos , Embarazo , Adulto Joven
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