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1.
Diagn Pathol ; 17(1): 48, 2022 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-35637541

RESUMO

INTRODUCTION: Malignant schwannoma is a malignant tumor of differentiation of Schwann cells or perineural cells. OBSERVATION: The patient was a 74-year-old woman with no particular pathological history. She presented swallowing difficulty of solids and odynophagia, evolving for 1 year. Physical examination revealed a budding tumor of the left palatine tonsil without cervical adenopathy. The CT scan confirmed the lesions and the absence of tumor extensions. Histological and immunohistochemical examination of the biopsy sample of the tonsil tumor concluded to be a malignant schwannoma. The patient underwent a tonsillectomy with postoperative follow-up. DISCUSSION: Malignant schwannomas are aggressive tumors. They usually occur in young adults. They mainly affect nerves and soft tissues. Occurrence in the amygdala is rare. CONCLUSION: The association of malignant schwannoma of the palatine tonsil and advanced age is rare.


Assuntos
Neurilemoma , Neurofibrossarcoma , Idoso , Feminino , Humanos , Neurilemoma/patologia , Neurilemoma/cirurgia , Tonsila Palatina/patologia , Tomografia Computadorizada por Raios X , Adulto Jovem
2.
ISRN Obstet Gynecol ; 2011: 242140, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21776398

RESUMO

Female genital schistosomiasis (FGS) is an isolated chronic form of schistosomiasis. Although most infections occur in residents of endemic areas, it has been clearly documented that brief freshwater exposure is sufficient to establish infection; thus, travellers may also be infected. The clinical manifestations of FGS are nonspecific, and lesions may mimic any neoplastic or infectious process in the female genital tract. It is important to take a careful history and physical examination, making sure to consider travel history in endemic areas. The diagnosis is confirmed by microscopy with egg identification or by serology. The standard of care for treatment is a single dose of oral praziquantel which avoids complications and substantial morbidity. Herein, we report a rare and original case of FGS in a European woman.

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