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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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References
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Journal ArticleDOI

Pulmonary epithelioid haemangioendothelioma in 21 patients, including three with partial spontaneous regression

TL;DR: This investigation studied the general conditions and prognostic factors of pulmonary epithelioid haemangioendothelioma, which is a rare disease, and three patients demonstrated partial spontaneous regression, and adverse prognostic features were identified.
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Nuclear Expression of CAMTA1 Distinguishes Epithelioid Hemangioendothelioma From Histologic Mimics

TL;DR: The diagnostic utility of immunohistochemistry for CAMTA1 in distinguishing EHE from histologic mimics, in particular benign epithelioid vascular tumors, epithelIOid angiosarcoma, and epitheliaid sarcoma is supported, an important distinction given the differences in biological potential and clinical course.
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Pathologic and clinical features of primary pulmonary extranodal marginal zone B-cell lymphoma of MALT type.

TL;DR: None of the following features predicted those patients who had an adverse outcome: systemic symptoms, presence of autoimmune disorders or paraproteinemia, anatomic distribution and number of pulmonary lesions, lymph node involvement, or presence of anthracycline-treated large B-cell lymphoma.
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