An Atypical Presentation of Childhood Paraganglioma with Seizures: A Case Report and Review of the Literature

Author:

Oyenusi Elizabeth Eberechi1ORCID,Nwigbo Uzoamaka Felicia2ORCID,Oladipo Oluwadamilola Moromoke2ORCID,Kene-Udemezue Blessing Ebele2ORCID,Akowundu Kasarachi Pauline2ORCID,Oleolo-Ayodeji Khadijah Omobusola2ORCID,Afoke Oluwaseun Adunni3ORCID,Babatunde Funmilayo Oluwatoyin2ORCID,Alakaloko Felix Makinde4ORCID,Asiyanbi Gabriel Kolawole5ORCID,Ogunleye Ezekiel Olayiwola6ORCID,Oduwole Abiola Olufunmilayo1ORCID,Lesi Foluso Ebun Afolabi7ORCID

Affiliation:

1. Endocrinology and Metabolism Unit, Department of Paediatrics, College of Medicine, University of Lagos, Lagos University Teaching Hospital, Lagos, Nigeria

2. Department of Paediatrics, Lagos University Teaching Hospital, Lagos, Nigeria

3. Department of Radiodiagnosis, Lagos University Teaching Hospital, Lagos, Nigeria

4. Paediatric Surgery Unit, Department of Surgery, Lagos University Teaching Hospital, Lagos, Nigeria

5. Department of Anaesthesia, College of Medicine, University of Lagos, Lagos University Teaching Hospital, Lagos, Nigeria

6. Cardiothoracic Unit, Department of Surgery, College of Medicine, University of Lagos, Lagos University Teaching Hospital, Lagos, Nigeria

7. Neurology Unit, Department of Paediatrics, College of Medicine, University of Lagos, Lagos University Teaching Hospital, Lagos, Nigeria

Abstract

Introduction. A paraganglioma (PGL) is a tumour derived from extra-adrenal chromaffin cells of the sympathetic paravertebral ganglia of the thorax, abdomen, and pelvis. Cardiovascular manifestations predominate but neurological symptoms like seizures can occur requiring a high index of suspicion for prompt diagnosis and treatment. Case Description. A 14-year-old girl was referred to the paediatric neurology unit for recurrent headaches of one-year duration, vomiting of 2 months duration, and an episode of generalized tonic-clonic seizures, 2 weeks prior to presentation. There was an associated history of impaired vision, palpitations, diaphoresis, and easy fatigability. Her blood pressure ranged from 150/101 to 160/120 mmHg. The brain CT scan was normal. ECG showed left ventricular hypertrophy. Abdominal USS revealed a right para-aortic mass necessitating 24-hour urine normetanephrine which was markedly elevated–1695.34 mcg/24 h (100–500). An abdominal CT scan confirmed a paraganglioma in the right para-aortic region. A multidisciplinary team consisting of paediatric endocrinologists, radiologists, anaesthetists, paediatric and cardiothoracic surgeons, and the intensive care unit (ICU) team was involved in the peri and postoperative management of the child. Intraoperative challenges were hypertension and hypotension (following tumour excision). She was nursed in the ICU for 48 hours. Histology results confirmed paraganglioma. Postoperative urine normetanephrines done a month after surgery had reverted to normal. Her blood pressure has remained normal 6 months after surgery, and no other symptoms have recurred. Conclusion. In evaluating aetiology of childhood hypertension, endocrine causes must be considered though they are rare. The occurrence of paraganglioma is uncommon and can present in unusual ways such as seizures. Measurement of blood pressure in children is advocated as part of routine health care. Clinicians must explore the aetiology of seizures and not merely control them with anticonvulsant therapy.

Publisher

Hindawi Limited

Subject

Endocrinology, Diabetes and Metabolism

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