Results 81 to 90 of about 539,143 (189)
Left: A 46‐year‐old non‐smoking female with a 2.4 cm right hilar mass (cT1cN0M0). Middle: Postoperative pathology reveals discordance between low proliferation (Ki‐67 < 2%) and unexpected focal lympho‐vascular invasion, with concomitant granulomatous inflammation. Right: After VATS lobectomy (pN0) and active surveillance, no recurrence occurred over 20
Qilian Wang +3 more
wiley +1 more source
Synchronous Primary Atypical Pulmonary Carcinoid and Cecal Adenocarcinoma: A Case Report
Pulmonary carcinoid tumors are a rare subgroup of neuroendocrine lung neo-plasms, accounting for approximately 1-2% of all primary lung cancers. The occurrence of synchronous primary malignancies involving pulmonary carcinoid and colorectal adeno ...
Gergov G. +5 more
doaj +1 more source
Primary ovarian mucinous carcinoid tumor: A case report and review of literature
Objective: Only a few cases of primary ovarian mucinous carcinoid tumor have been documented in the literature till date. We present a case of primary ovarian mucinous carcinoid tumor, atypical type, and review the reported cases.
Wen-Wei Hsu, Tsui-Lien Mao, Chi-Hau Chen
doaj +1 more source
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited condition affecting multiple endocrine organs, resulting in significant morbidity and decreased life expectancy.
L. Lou +4 more
semanticscholar +1 more source
This case describes a rare allodynia irAE induced by durvalumab in a patient with ES‐SCLC. It is a case of peripheral neuropathy, but the main manifestation differs from most previous cases. First, based on CT, ECG, and cardiac biomarker results, we ruled out cancer‐related pain and organic lesions.
Ruidan Li +6 more
wiley +1 more source
A 23-year-old man with multiple endocrine neoplasia type 1 (MEN 1) with pancreatic tail masses and Cushing syndrome (status after transsphenoidal adenomectomy) presented with a slow-growing, asymptomatic right lower lung lobe mass confirmed to be an ...
Ramtin Talebi +3 more
doaj +1 more source
Treatment of atypical pulmonary carcinoid with combination ipilimumab and nivolumab
Atypical pulmonary carcinoid (APC) is a lung neuroendocrine neoplasm (NEN), whose treatment draws from management of gastrointestinal NENs and small-cell lung carcinoma.
J. Nestor +3 more
semanticscholar +1 more source
Loss of Claudin‐18 (Cldn18) expression is a frequent and specific feature of non‐mucinous lung adenocarcinoma (NM‐LUAD). Cldn18 immunohistochemistry may serve as an ancillary tool for distinguishing malignant from non‐neoplastic alveolar epithelium, as well as for differentiating NM‐LUADs with mucin production from M‐LUADs, particularly in small or ...
Stefano Lucà +18 more
wiley +1 more source
Atypical carcinoid tumor of the larynx: a case report. [PDF]
Atypical carcinoid tumors of the larynx are rare and little known neoplasms, representing a diagnostic and therapeutic challenge. This article presents a clinical case of an atypical carcinoid tumor in a 48-year-old patient, who complained of ...
Mohamed HACHEMI +3 more
doaj +1 more source
ABSTRACT Background PLCNEC is a rare and highly aggressive lung cancer with a poor prognosis. Multimodal therapy, primarily chemotherapy‐based, is the standard for advanced PLCNEC, but the role of radiotherapy remains unclear. Methods We analyzed 1086 PLCNEC patients receiving chemotherapy from the Surveillance, Epidemiology, and End Results (SEER ...
Yuze Zhao +5 more
wiley +1 more source

