BACKGROUND Myoepithelial carcinoma(MC)is a rare malignant neoplasm that mainly occurs in the salivary gland.MC can be confused with many other tumors when arising outside the salivary glands because it presents with a...BACKGROUND Myoepithelial carcinoma(MC)is a rare malignant neoplasm that mainly occurs in the salivary gland.MC can be confused with many other tumors when arising outside the salivary glands because it presents with a wide spectrum of cytomorphological and immunohistochemical features.To the best of our knowledge,esophageal MC has not been previously reported.The purpose of this study was to describe the imaging and clinicopathological features of esophageal MC to improve the understanding of the disease.CASE SUMMARY Three men and one woman diagnosed with esophageal MC were enrolled in this study.The primary clinical symptom was dysphagia.The mass was mainly located in the middle esophagus.Laboratory tests revealed that two patients who underwent tumor abnormal protein were positive.Radical resection was performed for all patients with no adjuvant therapy.Hematoxylin-eosin staining showed infiltrative growth of epithelial cells with hyperchromatic and pleomorphic nuclei toward the periphery.Immunohistochemistry showed that all patients were positive for P63,and most patients were positive for SOX-10,AE1/AE3,P40,and calponin.The Ki-67 values were all higher than 60%.Patient one died one month after discharge from an unknown cause.Patient two lost to follow-up.At patient three’s four-month review,enhanced computed tomography(CT)showed anastomosis recurrence and bilateral lung metastases.He abandoned treatment and lost to follow-up.Patient four attended review appointments regularly and remained in a good general condition.CONCLUSION Here,we present the first report of esophageal MC and review the relevant literature.Esophageal MC is more likely to occur in the middle esophagus in older patients with male dominance.A fungating type observed on CT scanning may help narrow down the differential diagnosis.Cystic change or necrosis may occur in larger lesions.The final diagnosis should be made according to the pathological examination.The treatment for MC is surgical resection,and the efficacy of chemotherapy needs to be determined with future studies.展开更多
BACKGROUND Myoepithelial carcinoma(MC)is a clinically rare malignancy,there is controversy regarding its etiology and its biological behavior is not fully elucidated.Extensive surgical resection is the main treatment ...BACKGROUND Myoepithelial carcinoma(MC)is a clinically rare malignancy,there is controversy regarding its etiology and its biological behavior is not fully elucidated.Extensive surgical resection is the main treatment method.We describe a case of pleomorphic adenoma(PA)with multiple postoperative recurrences after malignant transformation,and the history of the disease in this patient was more than 20 years.Complete resection during the first surgery of PA and long-term postoperative follow-up is necessary.CASE SUMMARY A 34-year-old male with PA and a history of 5 postoperative recurrences over 21 years,each surgically removed,presented 15 d ago with headache,nasal congestion,protrusion of the right eyeball and loss of vision in the right eye,with progressively worsening symptoms.The patient underwent surgery,and MC was confirmed by pathology examination.A small PA component was locally visible under light microscope.The patient had a recurrence of the tumor 2 mo after surgery and underwent surgical resection.CONCLUSION During the first operation for PA,care should be taken not to rupture the envelope to prevent tumor cell implantation,and when complete resection is not possible due to the anatomical site,postoperative radiotherapy is necessary to control the lesion and prevent infiltration and malignant transformation of the tumor to MC.Computed tomography and magnetic resonance imaging is important for establishing diagnosis and developing a treatment plan.展开更多
We report a case of carcinoma ex pleomorphic adenoma of a sublingual gland in a 70-year-old man.Under a clinical diagnosis of benign salivary gland tumor,excision of the mass with the sublingual salivary gland in an e...We report a case of carcinoma ex pleomorphic adenoma of a sublingual gland in a 70-year-old man.Under a clinical diagnosis of benign salivary gland tumor,excision of the mass with the sublingual salivary gland in an en bloc fashion via an intraoral approach was performed.Histopathologically,there was a rupture of the fibrous capsule and diffuse cell-rich sheets composed of myoepithelial cells with round nuclei were also seen.Immunohistochemically,the cells that composed of cell rich sheets were positive to smooth muscle actin.Final diagnosis of myoepithelial carcinoma ex pleomorphic adenoma was made.展开更多
文摘BACKGROUND Myoepithelial carcinoma(MC)is a rare malignant neoplasm that mainly occurs in the salivary gland.MC can be confused with many other tumors when arising outside the salivary glands because it presents with a wide spectrum of cytomorphological and immunohistochemical features.To the best of our knowledge,esophageal MC has not been previously reported.The purpose of this study was to describe the imaging and clinicopathological features of esophageal MC to improve the understanding of the disease.CASE SUMMARY Three men and one woman diagnosed with esophageal MC were enrolled in this study.The primary clinical symptom was dysphagia.The mass was mainly located in the middle esophagus.Laboratory tests revealed that two patients who underwent tumor abnormal protein were positive.Radical resection was performed for all patients with no adjuvant therapy.Hematoxylin-eosin staining showed infiltrative growth of epithelial cells with hyperchromatic and pleomorphic nuclei toward the periphery.Immunohistochemistry showed that all patients were positive for P63,and most patients were positive for SOX-10,AE1/AE3,P40,and calponin.The Ki-67 values were all higher than 60%.Patient one died one month after discharge from an unknown cause.Patient two lost to follow-up.At patient three’s four-month review,enhanced computed tomography(CT)showed anastomosis recurrence and bilateral lung metastases.He abandoned treatment and lost to follow-up.Patient four attended review appointments regularly and remained in a good general condition.CONCLUSION Here,we present the first report of esophageal MC and review the relevant literature.Esophageal MC is more likely to occur in the middle esophagus in older patients with male dominance.A fungating type observed on CT scanning may help narrow down the differential diagnosis.Cystic change or necrosis may occur in larger lesions.The final diagnosis should be made according to the pathological examination.The treatment for MC is surgical resection,and the efficacy of chemotherapy needs to be determined with future studies.
文摘BACKGROUND Myoepithelial carcinoma(MC)is a clinically rare malignancy,there is controversy regarding its etiology and its biological behavior is not fully elucidated.Extensive surgical resection is the main treatment method.We describe a case of pleomorphic adenoma(PA)with multiple postoperative recurrences after malignant transformation,and the history of the disease in this patient was more than 20 years.Complete resection during the first surgery of PA and long-term postoperative follow-up is necessary.CASE SUMMARY A 34-year-old male with PA and a history of 5 postoperative recurrences over 21 years,each surgically removed,presented 15 d ago with headache,nasal congestion,protrusion of the right eyeball and loss of vision in the right eye,with progressively worsening symptoms.The patient underwent surgery,and MC was confirmed by pathology examination.A small PA component was locally visible under light microscope.The patient had a recurrence of the tumor 2 mo after surgery and underwent surgical resection.CONCLUSION During the first operation for PA,care should be taken not to rupture the envelope to prevent tumor cell implantation,and when complete resection is not possible due to the anatomical site,postoperative radiotherapy is necessary to control the lesion and prevent infiltration and malignant transformation of the tumor to MC.Computed tomography and magnetic resonance imaging is important for establishing diagnosis and developing a treatment plan.
文摘We report a case of carcinoma ex pleomorphic adenoma of a sublingual gland in a 70-year-old man.Under a clinical diagnosis of benign salivary gland tumor,excision of the mass with the sublingual salivary gland in an en bloc fashion via an intraoral approach was performed.Histopathologically,there was a rupture of the fibrous capsule and diffuse cell-rich sheets composed of myoepithelial cells with round nuclei were also seen.Immunohistochemically,the cells that composed of cell rich sheets were positive to smooth muscle actin.Final diagnosis of myoepithelial carcinoma ex pleomorphic adenoma was made.
