BACKGROUND Primary schwannoma is a rare submucosal tumor of the esophagus,which is most often benign,and surgery is the only effective treatment.So far,only a few cases have been reported.Herein,we reported a single c...BACKGROUND Primary schwannoma is a rare submucosal tumor of the esophagus,which is most often benign,and surgery is the only effective treatment.So far,only a few cases have been reported.Herein,we reported a single case diagnosed with primary esophageal schwannoma that was totally removed by submucosal tunneling endoscopic resection(STER).CASE SUMMARY A 62-year-old man presented to the hospital with a history of resection of a malignant gastric tumor and mild dysphagia.Endoscopic examination revealed a large submucosal elevated lesion in the esophagus 25-30 cm from the incisors.Endoscopic ultrasonography detected a 45 mm×35 mm×31 mm hypoechoic lesion;chest computed tomography showed a mass of approximately 55 mm×35 mm×29 mm.A preliminary examination showed features suggestive of a stromal tumor.Pathological findings indicated esophageal schwannoma.Next,STER alone was performed to completely resect the mass,and the patient recovered well post-surgery.Afterward,the patient was discharged and showed no tumor recurrence at 33 mo of follow-up.CONCLUSION Endoscopic resection is still an effective treatment for large esophageal schwannomas(>30 mm)under meticulous morphological evaluation.展开更多
BACKGROUND Hemangioblastoma typically occurs in the cerebellum,spinal cord,and central nervous system.However,in rare cases,it could occur in the retina or optic nerve.The prevalence of retinal hemangioblastoma is 1 i...BACKGROUND Hemangioblastoma typically occurs in the cerebellum,spinal cord,and central nervous system.However,in rare cases,it could occur in the retina or optic nerve.The prevalence of retinal hemangioblastoma is 1 in 73080,and it occurs either alone or as the manifestation of von Hippel Lindau(VHL)disease.Here,we reported a rare case with the imaging features of retinal hemangioblastoma without VHL syndrome,along with the relevant literature review.CASE SUMMARY A 53-year-old man had progressive swelling,pain and blurred vision in the left eye without obvious inducement for 15 d.Ultrasonography revealed a possible optic nerve head melanoma.Computed tomography(CT)showed punctate calcification on the posterior wall of the left eye ring and small patchy soft tissue density in the posterior part of the eyeball.Magnetic resonance imaging showed slightly hyperintense signal on T1-weighted images and slightly hypointense-toisointense signal on T2-weighted images at the medial and posterior edges of the left eyeball,a significant enhancement was observed in the contrast-enhanced scans.Positron emission tomography/CT fusion images showed that the glucose metabolism of the lesion was normal.Pathology was consistent with hemangioblastoma.CONCLUSION Early identification of retinal hemangioblastoma based on imaging features is of great value for its personalized treatment.展开更多
BACKGROUND Previous studies reported that most of the intracranial dermoid cyst ruptures were spontaneous,and only a few were traumatic,with asymptomatic much rarer than the symptomatic ruptures.Hence,how to deal with...BACKGROUND Previous studies reported that most of the intracranial dermoid cyst ruptures were spontaneous,and only a few were traumatic,with asymptomatic much rarer than the symptomatic ruptures.Hence,how to deal with the asymptomatic traumatic rupture of intracranial dermoid cyst remains a challenge in the clinic.CASE SUMMARY A 59-year-old man was accidentally diagnosed with intracranial dermoid cyst through a cranial computed tomography(CT)scan due to a car accident.A mixed-density lesion with fat and a calcified margin was observed in the midline of the posterior fossa,accompanied with lipid droplet drifts in brain sulci,fissures,cisterns,and ventricles.After 1 wk of conservative observation,no change was observed on the updated cranial CT scan.After 2 wk of conservative observation,magnetic resonance imaging examination confirmed that the lesion was a traumatic rupture of a posterior fossa dermoid cyst with lipid droplet drifts.As the patient exhibited no adverse symptoms throughout the 2 wk,a 6-mo follow-up visit was arranged for him instead of aggressive treatment.Nonetheless,the patient did not show any abnormal neurological symptoms in the 6 mo of follow-up visits.CONCLUSION Asymptomatic traumatic rupture of intracranial dermoid cyst could be just followed or treated conservatively rather than treated aggressively.展开更多
基金Supported by National Natural Science Foundation of China,No.81871337Medical and Health Science and Technology Projects of Zhejiang Province,No.2019KY117.
文摘BACKGROUND Primary schwannoma is a rare submucosal tumor of the esophagus,which is most often benign,and surgery is the only effective treatment.So far,only a few cases have been reported.Herein,we reported a single case diagnosed with primary esophageal schwannoma that was totally removed by submucosal tunneling endoscopic resection(STER).CASE SUMMARY A 62-year-old man presented to the hospital with a history of resection of a malignant gastric tumor and mild dysphagia.Endoscopic examination revealed a large submucosal elevated lesion in the esophagus 25-30 cm from the incisors.Endoscopic ultrasonography detected a 45 mm×35 mm×31 mm hypoechoic lesion;chest computed tomography showed a mass of approximately 55 mm×35 mm×29 mm.A preliminary examination showed features suggestive of a stromal tumor.Pathological findings indicated esophageal schwannoma.Next,STER alone was performed to completely resect the mass,and the patient recovered well post-surgery.Afterward,the patient was discharged and showed no tumor recurrence at 33 mo of follow-up.CONCLUSION Endoscopic resection is still an effective treatment for large esophageal schwannomas(>30 mm)under meticulous morphological evaluation.
基金Supported by the National Natural Science Foundation of China,No.81871337the Natural Science Foundation of Zhejiang Province,No.LY16H180007。
文摘BACKGROUND Hemangioblastoma typically occurs in the cerebellum,spinal cord,and central nervous system.However,in rare cases,it could occur in the retina or optic nerve.The prevalence of retinal hemangioblastoma is 1 in 73080,and it occurs either alone or as the manifestation of von Hippel Lindau(VHL)disease.Here,we reported a rare case with the imaging features of retinal hemangioblastoma without VHL syndrome,along with the relevant literature review.CASE SUMMARY A 53-year-old man had progressive swelling,pain and blurred vision in the left eye without obvious inducement for 15 d.Ultrasonography revealed a possible optic nerve head melanoma.Computed tomography(CT)showed punctate calcification on the posterior wall of the left eye ring and small patchy soft tissue density in the posterior part of the eyeball.Magnetic resonance imaging showed slightly hyperintense signal on T1-weighted images and slightly hypointense-toisointense signal on T2-weighted images at the medial and posterior edges of the left eyeball,a significant enhancement was observed in the contrast-enhanced scans.Positron emission tomography/CT fusion images showed that the glucose metabolism of the lesion was normal.Pathology was consistent with hemangioblastoma.CONCLUSION Early identification of retinal hemangioblastoma based on imaging features is of great value for its personalized treatment.
文摘BACKGROUND Previous studies reported that most of the intracranial dermoid cyst ruptures were spontaneous,and only a few were traumatic,with asymptomatic much rarer than the symptomatic ruptures.Hence,how to deal with the asymptomatic traumatic rupture of intracranial dermoid cyst remains a challenge in the clinic.CASE SUMMARY A 59-year-old man was accidentally diagnosed with intracranial dermoid cyst through a cranial computed tomography(CT)scan due to a car accident.A mixed-density lesion with fat and a calcified margin was observed in the midline of the posterior fossa,accompanied with lipid droplet drifts in brain sulci,fissures,cisterns,and ventricles.After 1 wk of conservative observation,no change was observed on the updated cranial CT scan.After 2 wk of conservative observation,magnetic resonance imaging examination confirmed that the lesion was a traumatic rupture of a posterior fossa dermoid cyst with lipid droplet drifts.As the patient exhibited no adverse symptoms throughout the 2 wk,a 6-mo follow-up visit was arranged for him instead of aggressive treatment.Nonetheless,the patient did not show any abnormal neurological symptoms in the 6 mo of follow-up visits.CONCLUSION Asymptomatic traumatic rupture of intracranial dermoid cyst could be just followed or treated conservatively rather than treated aggressively.
基金Project supported by the National Natural Science Foundation of China(No.81771158)the Science Foundation of the Health Commission of Zhejiang Province(Nos.2016147373 and 2019321345),China
