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Primary lung neoplasms presenting as multiple synchronous lung nodules

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TLDR
Several rare primary lung neoplasms that originate from epithelial, mesenchymal and lymphoid tissues of the lung present as multiple synchronous indeterminate lung nodules on chest CT merit increased awareness among radiologists, pathologists and pulmonologists, as well as a multidisciplinary team approach.
Abstract
Multiple synchronous lung nodules are frequently encountered on computed tomography (CT) scanning of the chest and are most commonly either non-neoplastic or metastases from a known primary malignancy. The finding may initiate a search for primary malignancy elsewhere in the body. An exception to this rule, however, is a class of rare primary lung neoplasms that originate from epithelial (pneumocytes and neuroendocrine), mesenchymal (vascular and meningothelial) and lymphoid tissues of the lung. While these rare neoplasms also present as multiple synchronous unilateral or bilateral lung nodules on chest CT, they are often overlooked in favour of more common causes of multiple lung nodules. The correct diagnosis may be suggested by a multidisciplinary team and established on biopsy, performed either as part of routine diagnostic work-up or staging for malignancy. In this review, we discuss clinical presentations, imaging features, pathology findings and subsequent management of these rare primary neoplasms of the lung.

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Diffuse Idiopathic Neuroendocrine Cell Hyperplasia: An Interstitial Lung Disease With Airway Obstruction

TL;DR: Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) is a rare clinicopathologic syndrome with little known of its clinical course and treatment options.
Journal ArticleDOI

Pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma with multiple thin-walled pulmonary cysts: a case report and review of the literature.

TL;DR: The case of a previously healthy 58-year-old Japanese woman with a rare case of pulmonary mucosa-associated lymphoid tissue (p-MALT) lymphoma with multiple cystic lesions suggests that the possibility of p-Malt lymphoma should be considered in patients with multiple Cystic lung diseases.
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TL;DR: It is important to maintain a high index of suspicion for this disorder so that appropriate treatment can be instituted, and to focus on the acute and follow-up central nervous system findings of the disease, especially in children.
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