SESSION TITLE: Medical Student/Resident Lung Cancer Posters SESSION TYPE: Med Student/Res Case Rep Postr PRESENTED ON: October 18-21, 2020 INTRODUCTION: We present a case of a 29-year-old female with an insidious clinical presentation. At first, it was thought to be an infectious disease, but it turned out to be a very rare neoplasm. CASE PRESENTATION: 29-year-old female with healthcare-related tuberculosis exposure for working as a nurse in an emergency service and homecare. She had a 2-month history of non-productive cough and progressive dyspnea, progressing from exertion to small effort dyspnea. She visited an emergency service where a chest x-ray was obtained. It showed multiple, diffuse, bilateral, micronodular radiopacities, therefore, being referred to a Respiratory Medicine Facility for further studies. On arrival, a High-Resolution Computed Tomography (HRCT) of the lungs was performed, which showed the previously mentioned nodules as well as interlobular septal thickening. A flexible video bronchoscopy (FBO) was then performed, obtaining specimens samples of bronchial lavage for AFB, PCR for M. tuberculosis and transbronchial biopsies. The first two were reported as “negative”, and the transbronchial biopsies reported “nodular and diffuse fibrosis”, therefore proceeding to a surgical biopsy, with the following findings: “generalized micronodular pattern and multiple nodules. A surgical specimen from lingula is obtained”. Histopathology reported: “Low-grade vascular neoplasm compatible, by morphology, with Epithelioid Hemangioendothelioma. Immunohistochemistry positive to CD31 and CD 34, and negative to Actin, CK and COCKTEL.” DISCUSSION: The suspicion of an infectious disease was based on clinical findings: A young woman from a tuberculosis endemic region in México, with an important tuberculosis exposure due to her work as a healthcare professional, a clinical condition of 2-month non-productive cough, and a HRCT with micronodular hyperdensities. At first glance, Miliary Tuberculosis was suspected and accordingly approached. All tests made in fiber-optic bronchoscopy were negative for Tuberculosis and Fungi. Afterward, when a surgical biopsy was performed a neoplasm was found. Oncology assessed the case and decided expectant follow up. The patient will maintain follow up every 3 months with an HRCT. In the event of progression or worsening of the symptoms, medical therapy will be started. CONCLUSIONS: The epithelioid hemangioendothelioma is a very rare low-grade sarcoma. It appears typically in young women, with an average age of 40 years. An insidious evolution if often present, with respiratory symptoms, nodules, usually under 1cm, and interlobular septal thickening in the HRCT. The treatment consists of chemotherapy, interleukin-2 and interferon alfa-2B. The average survival of this neoplasm is 4.6 years, varying between 12 months and 26 years. Reference #1: Cronin P, Arenberg D. Pulmonary Epithelioid Hemangioendothelioma An Unusual Case and a Review of the Literature. 2nd ed. CHEST; 2004. Reference #2: Rosengarten D, Kramer M, Amir G, Fuks L, Berkman N. Hemangioendothelioma Epithelioid Pulmonary. 13th ed. IMAJ, Israel Medical Association Journal; 2011. DISCLOSURES: No relevant relationships by Paloma Barajas, source=Web Response No relevant relationships by Luis Galindo, source=Web Response No relevant relationships by Maria del Carmen Lozano Cuevas, source=Web Response No relevant relationships by Alfredo Noyola Correa, source=Web Response
Read full abstract