2014
DOI: 10.1097/rct.0b013e3182ab21fe
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Primary Small Cell Neuroendocrine Carcinoma of the Mediastinum

Abstract: A large tumor located in the anterior-middle mediastinum, showing scattered punctate calcifications and compressing or invading the adjacent mediastinal structures, should arouse suspicion for a small cell neuroendocrine carcinoma. However, the diagnosis of such tumors requires a combination of pathological and immunohistochemical examination.

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Cited by 9 publications
(4 citation statements)
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“…However, mediastinal primary SCC is extremely rare. Its origin is not clear (20). The tumor cells could synthesize, store, and release peptide or amine hormones such as gastrin and chromogranin.…”
Section: Discussionmentioning
confidence: 99%
“…However, mediastinal primary SCC is extremely rare. Its origin is not clear (20). The tumor cells could synthesize, store, and release peptide or amine hormones such as gastrin and chromogranin.…”
Section: Discussionmentioning
confidence: 99%
“…With only a few cases currently documented in the literature, the etiology of MSCNC remains unknown. These types of tumors are frequently discovered secondary to their compression of neighboring mediastinal structures [1]. Diagnosis requires both pathological identification via biopsy revealing the characteristic organoid pattern as well as immunohistochemical positivity for characteristic markers of MSCNC, including chromogranin A, synaptophysin, and neuron-specific enolase, among others [2].…”
Section: Introductionmentioning
confidence: 99%
“…However, mediastinal primary small cell neuroendocrine carcinoma (MPSCN) is extremely rare. Its origin is not clear [ 2 ]. The diagnosis of MPSCN requires a combination of pathological and immunohistochemical examination.…”
mentioning
confidence: 99%
“…Most patients have retrosternal pain, dry cough, or dyspnoea, which can occur because of mass effects. Obstruction of the superior vena cava could cause superior vena cava syndrome [ 2 ].…”
mentioning
confidence: 99%