Rare Mesenchymal Tumors
Mesenchymal neoplasms including leiomyoma, lipoma, chondroma, and a variety of neural tumors rarely occur as primary lung neoplasms. Their histopathologic features are similar to those of the same tumors in other locations.
Part 1 Leiomyoma
Donna M. Coffey
Leiomyomas primary to the lung are rare endobronchial or parenchymal neoplasms. Endobronchial leiomyomas may present with obstructive symptoms. Differential diagnosis includes hamartomas, low-grade leiomyosarcomas (primary and metastatic), spindle-cell carcinoid, and solitary fibrous tumor.
Part 2 Lipoma
Alvaro C. Laga
Timothy C. Allen
Keith M. Kerr
Philip T. Cagle
Pulmonary lipomas are rare predominantly endobronchial neoplasms that may, due to their polypoid nature, occlude the bronchial lumen. Differential diagnosis includes lipomatous hamartoma.
Part 3 Chondroma
Helmut Popper
Chondromas are benign tumors composed of hyaline cartilage. They have been reported in association with the Carney triad, which consists of gastric stroma sarcoma, paraganglioma, and pulmonary chondroma. They are generally asymptomatic and may present radiologically with “popcorn” calcification.
Histologic Features
Well-defined lobular masses composed of hypocellular hyaline cartilage.
No features of malignancy.
Components of hamartoma such as adipose tissue and entrapped respiratory epithelium are absent.
![]() Figure 24.4 Chondroma of the lung shows cartilage lacking adipose tissue, entrapped respiratory epithelium, or other components of a hamartoma. |
Part 4 Neural and Related Tumors
Primary pulmonary neural neoplasms include granular-cell tumor, schwannoma, neurofibroma, and ganglioneuroma. All of these are very rare as lung primaries. Meningioma primary in the lung is extremely rare, although minute meningothelial-like nodules (see Chapter 20) are common by comparison. Rarely, meningioma may metastasize to the lung. All of these tumors exhibit the same histopathology as neural and related tumors in other locations.

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