papilloma/vomiting

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A squamous cell papilloma as a cause of dysphagia and vomiting.

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Squamous cell papillomas occur relatively commonly intra-orally. Patients are usually unaware of their presence. A case is described of a squamous cell papilloma arising from the uvula, which presented as an unusual cause of dysphagia and vomiting.

Vomiting with depression: choroid plexus papilloma.

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Purely cystic form of choroid plexus papilloma with acute hydrocephalus in an infant. Case report.

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Infants with acute hydrocephalus often present with nonspecific neurological signs, and cystic choroid plexus papilloma (CPP) is a very rare cause of acute obstructive hydrocephalus. The authors present the case of a 1-year-old girl who became irritable, started vomiting, and became comatose within

Intraductal growth-type mucin-producing peripheral cholangiocarcinoma associated with biliary papillomatosis.

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A 64-year-old woman with upper abdominal pain, nausea, and vomiting was admitted. The magnetic resonance imaging revealed marked dilation and "crowding" of the segment 4 bile ducts with an area suspicious for a stone or tumor. Ultrasonography-guided percutaneous transhepatic cholangiography revealed

The use of a double-lumen central venous catheter for airway management in pediatric patients undergoing laryngeal papillomatosis surgery.

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OBJECTIVE To evaluate the efficacy and safety of a spontaneous ventilation anesthesia technique with insufflation of oxygen and volatile agent through a double-lumen central venous catheter (DLCVC) in pediatric patients undergoing suspension laryngoscopic surgery for laryngeal

Choroid plexus papilloma of the fourth ventricle.

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A 14 year old girl presented with a 6 months' history of headache with vomiting, ataxia and cerebellar signs. CT and MRI revealed obstructive hydrocephalus secondary to a large fourth ventricular mass which enhanced markedly on contrast administration. Histopathology of the resected mass revealed

Lesson of the month 2: A choroid plexus papilloma manifesting as anorexia nervosa in an adult.

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A Caucasian female previously diagnosed with anorexia nervosa was referred by psychiatric services to the general medical team. She presented with dehydration, vomiting, weakness, a body mass index of 13 kg/m2 and was treated with intravenous and enteral supplementation. During admission her

Diffuse arachnoidal enhancement of a well differentiated choroid plexus papilloma.

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BACKGROUND The case of a 38-year old man with a histologically benign choroid plexus papilloma arising within the fourth ventricle with en plaque growth around the brain stem and medulla is described in detail. Up to this point this particular growth pattern has not been published and is a rare

[Malignant choroid plexus papilloma. An autopsy case report (author's transl)].

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Malignant choroid plexus papilloma is a rare disease. The autopsy case of malignant choroid plexus papilloma being suggestive of the youngest in Japan, was reported. This 8-months-old baby had normal delivery history, and the development and growth were not eventful. The patient admitted to the

Endoscopic removal of a cystic choroid plexus papilloma of the third ventricle: a case report and review of the literature.

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Cystic choroid plexus papilloma (CPP) of the third ventricle is rare. The authors have reported a case of cystic CPP resected successfully through neuroendoscopic approach. An 18-year-old young man was admitted to our hospital, presented with blurred vision and paroxysmal, intermittent, severe

Metachronous Type I pleuropulmonary blastoma and atypical choroid plexus papilloma in a young child.

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Pleuropulmonary blastoma (PPB) is a rare childhood tumor, often associated with germline DICER1 mutations and a risk for development of other benign and malignant tumors, a constellation termed DICER1 syndrome. A 1-year-old male was diagnosed with Type I PPB and screened regularly thereafter for

An unusual location for a choroid plexus papilloma: the pineal region.

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OBJECTIVE Choroid plexus papillomas (CPP) are rare benign neoplasms of the central nervous system that occur most often in children during the first decade of life. They occur most often in the lateral ventricle. It is extremely rare for a CPP to occur in the pineal region. We describe the case of a

Unusual localization of a choroid plexus papilloma in a 4-year-old female.

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Choroid plexus papillomas are rare tumors that are confined to areas in which the choroid plexus is normally located. In children, choroid plexus papillomas are predominantly located in the lateral ventricles. Clinically they present with signs of raised intracranial pressure, such as vomiting and

Squamous cell papilloma of the esophagus in a child.

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The case of a 17 month-old girl with an esophageal squamous cell papilloma is presented. There was a previous history of intermittent hematemesis and vomiting. The tumors were located in the lower esophagus and were removed operatively. Our patient is the youngest case reported so far.

Choroid plexus papilloma in a 4-month-old child: a case report.

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We report a case of choroid plexus papilloma arising from the right lateral ventricle in a 4-month-old infant. Because of intermittent vomiting, abdominal pain, and diarrhea, the child was initially treated with intravenous rehydration, which aggravated the symptoms, and a bulging fontanel

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