Flyer

Health Science Journal

  • ISSN: 1108-7366
  • Journal h-index: 47
  • Journal CiteScore: 16.17
  • Journal Impact Factor: 2.63
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days
Reach us +441518081309
20+ Million Readerbase
Indexed In
  • Genamics JournalSeek
  • China National Knowledge Infrastructure (CNKI)
  • CiteFactor
  • CINAHL Complete
  • Scimago
  • Electronic Journals Library
  • Directory of Research Journal Indexing (DRJI)
  • EMCare
  • OCLC- WorldCat
  • University Grants Commission
  • Geneva Foundation for Medical Education and Research
  • Euro Pub
  • Google Scholar
  • Secret Search Engine Labs
Share This Page

Primary Hepatic Lymphoma: An often Missed Diagnosis

XX Congresso Regionale FADOI CAMPANIA: Non ci siamo mai fermati
Italy 2021

De Donato MT, Renis M*, Tripodi MF, De Siervi P, Salvatore V and Persico M

Clinica Medica ed Epatologia, AOU ├ó┬?┬?San Giovanni di Dio e Ruggi d├ó┬?┬?Aragona├ó┬?┬Ł Salerno, Italy
Medicina Interna, P.O Cava AOU ├ó┬?┬?San Giovanni di Dio e Ruggi d├ó┬?┬?Aragona├ó┬?┬Ł Salerno, Italy

Posters & Accepted Abstracts: Health Sci J

Abstract:

Background: Primary hepatic lymphoma (PHL) is a rare form of non-Hodgkin's lymphoma that causes significant diagnostic difficulties. Case report: Male 85-Year-Old Hospitalized for fatigue, weight loss, and eventually jaundice. Ultrasound evidence, fully confirmed by CT: "Enlarged liver, with subverted ultrasound structure due to multiple hypoechoic nodules of various sizes, spread over the entire parenchyma, which may be referred to secondary lesions". After a long series of investigations, only the liver biopsy allowed the definitive diagnosis of PHL. Discussion: Hepatic lymphoma can be distinguished into primary and secondary. To be classified as PHL, this disease must be confined to the liver and hilum lymphnodes, with no distant involvement (spleen, bone marrow, or other lymphoid sites). PHL is rare. Symptoms are non-specific, as are laboratory and instrumental tests and imaging techniques. Due to the low incidence and the absence of specific symptoms, patients with PHL often go through a long and frustrating diagnostic process before arriving at a definitive diagnosis, which is often missed. A differential diagnosis with other space-occupying liver lesions should be made. Liver biopsy, often performed late, is the investigation that allows the right diagnosis, also supported by the absence of extrahepatic lymphoproliferative involvement.