Intrapulmonary Schwannoma: A Rare Case Report and Review of the Literature

Schwannoma is a benign, well-circumscribed, and encapsulated peripheral nerve sheath tumor that develops from Schwann cells. The growth pattern is usually slow, tending to clinical indolence. Primary pulmonary neuronal tumors are very rare, accounting for ~0.2% of all lung neoplasms, and are often misdiagnosed due to their nonspecific radiological features. A 50-year-old man presented with a large cystic mass in upper lobe of left lung discovered incidentally on chest X-ray during work up after a blunt chest trauma. Gross examination of the mass following surgical excision revealed a well-circumscribed, encapsulated creamy-gray cystic lesion with gelatinous material measuring 10.5 × 6 × 5.5 cm, attached to a segment of lung. Microscopically, the tumor showed hypo- and hypercellular areas with proliferation of elongated wavy cells in a myxoid background which is characteristic of Schwannoma. Despite intrapulmonary schwannomas' rarity, it is essential to consider schwannomas in the differential diagnosis of pulmonary masses, particularly when clinical and radiological findings suggest a well-defined, encapsulated lesion.

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Publication Details

Journal
Sage Open Pathology
Published
2025-12-01
DOI
https://doi.org/10.1177/30502098251410398
Citations
1
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
1.39
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article

Intrapulmonary Schwannoma: A Rare Case Report and Review of the Literature

Zahra Beyzaei, Parviz Mardani, Mehdi Jamalpour, Bita Geramizadeh et al.
1 citations
Sage Open Pathology
Neurofibromatosis and Schwannoma Cases
1.39
article

Intrapulmonary Schwannoma: A Rare Case Report and Review of the Literature

Zahra Beyzaei, Parviz Mardani, Mehdi Jamalpour, Bita Geramizadeh, Elham EntezarAlmahdi
article en
1 citations

Abstract

Schwannoma is a benign, well-circumscribed, and encapsulated peripheral nerve sheath tumor that develops from Schwann cells. The growth pattern is usually slow, tending to clinical indolence. Primary pulmonary neuronal tumors are very rare, accounting for ~0.2% of all lung neoplasms, and are often misdiagnosed due to their nonspecific radiological features. A 50-year-old man presented with a large cystic mass in upper lobe of left lung discovered incidentally on chest X-ray during work up after a blunt chest trauma. Gross examination of the mass following surgical excision revealed a well-circumscribed, encapsulated creamy-gray cystic lesion with gelatinous material measuring 10.5 × 6 × 5.5 cm, attached to a segment of lung. Microscopically, the tumor showed hypo- and hypercellular areas with proliferation of elongated wavy cells in a myxoid background which is characteristic of Schwannoma. Despite intrapulmonary schwannomas' rarity, it is essential to consider schwannomas in the differential diagnosis of pulmonary masses, particularly when clinical and radiological findings suggest a well-defined, encapsulated lesion.

Sage Open PathologyVol. 18
Shiraz University of Medical Sciences (IR)
Good health and well-being
Openalex Percentile: Top 13%
Neurofibromatosis and Schwannoma Cases
1.39
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