Combined exploratory laparotomy, transpsoas, and thoracic approach to resection of a giant spinal ganglioneuroma: illustrative case

BACKGROUND Ganglioneuromas are rare peripheral nervous system tumors of neural crest origin. Most are often asymptomatic and incidentally found, but large tumors can cause mass effect. Herein, the authors report a case of a giant ganglioneuroma that arose from the lumbar foramina into the retroperitoneal and thoracic cavities. OBSERVATIONS A 62-year-old female presented with low back pain, left lower extremity swelling, and increased sensation of an abdominal mass. Surgical treatment options were reviewed with the patient and coordinated care was planned by surgical oncological specialists. The patient opted for multistage exploratory laparotomy for abdominal mobilization, diaphragm resection, and en bloc resection with neuromonitoring. After surgery, the patient experienced significant improvement in symptoms. LESSONS A combined surgical exposure involving gastrointestinal, thoracic, and neurological surgeons can be important in the safe resection of ganglioneuromas that span multiple body cavities. Hence, a thorough preoperative assessment could help plan surgery accordingly.

[1]  Erfan Tasdighi,et al.  Primary Spinal Tumors and Masses in Children , 2022, Iranian journal of child neurology.

[2]  H. Sarnat,et al.  Ganglion cell maturation in peripheral neuroblastic tumours of children. , 2022, Clinical neuropathology.

[3]  M. Teixeira,et al.  Robotic and standard surgical intervention as adjunct therapies for retroperitoneal ganglioneuroma resection: a case report , 2021, BMC Surgery.

[4]  W. Young,et al.  Presentation and outcomes of adrenal ganglioneuromas: A cohort study and a systematic review of literature , 2021, Clinical endocrinology.

[5]  P. Baláž,et al.  Oncovascular Resection of a Ganglioneuroma Involving the Coeliac Trunk and Hepatic Artery—A Case Report , 2021, Vascular and endovascular surgery.

[6]  R. Bedir,et al.  An urban legend: Malignant transformation caused by radiotherapy in patients with presacral ganglioneuroma. The necessity and first-time administration of radiotherapy. Case report and literature review , 2021, Journal of cancer research and therapeutics.

[7]  V. Alibegovic,et al.  Total resection of a giant retroperitoneal and mediastinal ganglioneuroma—case report and systematic review of the literature , 2020, World Journal of Surgical Oncology.

[8]  H. Lehnert,et al.  Ganglioneuromas across age groups: Systematic review of individual patient data , 2020, Clinical endocrinology.

[9]  Peng Cheng,et al.  Bilateral and symmetric C1-C2 dumbbell ganglioneuromas associated with neurofibromatosis type 1: A case report , 2019, World journal of clinical cases.

[10]  G. Tekant,et al.  Adrenal masses in children: Imaging, surgical treatment and outcome. , 2019, Asian journal of surgery.

[11]  K. Sapalidis,et al.  Laparoscopic Excision of an Adrenal Ganglioneuroma Presented as an Incindentaloma of the Retro Peritoneum , 2018, Current health sciences journal.

[12]  Shao-Song Tu,et al.  Ganglioneuroma in unusual sites: clinical, radiologic and pathological features. , 2018, International journal of clinical and experimental pathology.

[13]  Y. J. Chai,et al.  Clinicopathological Features of Ganglioneuroma Originating From the Adrenal Glands , 2016, World Journal of Surgery.

[14]  N. Kikuno,et al.  Retroperitoneal catecholamine-producing ganglioneuroma with a birth history of monozygotic twins who both suffered from neuroblastoma during their childhoods: A case report with genome analysis , 2015, Journal of the Neurological Sciences.

[15]  D. Linos,et al.  Adrenal ganglioneuromas: incidentalomas with misleading clinical and imaging features. , 2011, Surgery.

[16]  M. Carella,et al.  Multiple spinal ganglioneuromas in a patient harboring a pathogenic NF1 mutation , 2010, Clinical genetics.

[17]  G. Papastratis,et al.  Laparoscopic Resection of Large Adrenal Ganglioneuroma , 2007, JSLS : Journal of the Society of Laparoendoscopic Surgeons.

[18]  C. Pan,et al.  Malignant ganglioneuroma arising from mediastinal mixed germ cell tumor. , 2007, Journal of the Chinese Medical Association : JCMA.

[19]  J. Moley,et al.  Adrenal ganglioneuromas in children with multiple endocrine neoplasia type 2: a report of two cases. , 2005, The Journal of clinical endocrinology and metabolism.

[20]  F. Berthold,et al.  Metabolic activity and clinical features of primary ganglioneuromas , 2001, Cancer.

[21]  U. Mödder,et al.  Ganglioneurome im Kindesalter: CT- und MRT-Charakteristika , 2000 .

[22]  M. Tötsch,et al.  Chromogranin A, secretogranin II and vasoactive intestinal peptide in phaeochromocytomas and ganglioneuromas , 1993, Histopathology.

[23]  J. Markisz,et al.  MRI characteristics of two cases of adrenal ganglioneuromas. , 1992, Clinical imaging.

[24]  D. Harwood-Nash,et al.  CT of neuroblastomas and ganglioneuromas in children. , 1982, AJR. American journal of roentgenology.