Ganglioneuroma
Key Facts
Terminology
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Ganglioneuroma (GN)
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Benign tumor of neural origin
Clinical Issues
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Incidence
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Tumor is more common in young patients
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Location
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More common in posterior mediastinum
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Symptomatology
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Chest pain
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Horner syndrome
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Shortness of breath
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Neurofibromatosis
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Treatment
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Surgical resection
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Prognosis
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Good
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Clinical features
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Tumor is more common in younger patients
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More common in posterior mediastinum
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Shortness of breath
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Symptoms
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Shortness of breath
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Chest pain
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Horner syndrome
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Neurofibromatosis
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Top Differential Diagnoses
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Schwannoma
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Neurofibroma
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Ganglioneuroblastoma
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Solitary fibrous tumor
TERMINOLOGY
Abbreviations
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Ganglioneuroma (GN)
Definitions
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Benign tumor of neural origin
ETIOLOGY/PATHOGENESIS
Etiology
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There is no definitive etiology for this neoplasm
CLINICAL ISSUES
Epidemiology
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Incidence
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Unusual tumors representing a small percentage of mediastinal tumors
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Age
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More common in younger patients
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Site
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GN is more common in posterior mediastinum
Presentation
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Shortness of breath
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Chest pain
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Horner syndrome
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Neurofibromatosis
Treatment
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Surgical approaches
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Complete surgical resection
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Prognosis
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Good
MACROSCOPIC FEATURES
General Features
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Well circumscribed and encapsulated
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Firm, gray to yellowish
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Cut surface shows whitish smooth or whorled appearance
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Areas of necrosis and hemorrhage are generally absent
Size
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Tumors vary in size from 1 cm to > 10 cm in greatest dimension
MICROSCOPIC PATHOLOGY
Histologic Features
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Mature ganglion cells embedded in loose fibrocollagenous or subtle spindle cell stroma
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Proliferation of Schwann cells, nerve fibers, and ganglion cells
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Nissl granules may be seen in some cases in ganglion cells
Cytologic Features
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Mature ganglion cells
DIFFERENTIAL DIAGNOSIS
Schwannoma
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Classically shows Antoni A and B areas while these would be unusual in GN
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It would be unusual for Schwannoma to show numerous ganglion cells
Neurofibroma
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Spindle cell component of neurofibroma is similar to that of GN
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Neurofibromas lack the presence of ganglion cells
Ganglioneuroblastoma
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Shows neuroblastomatous component, which is absent in GN
Solitary Fibrous Tumor

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