<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.4 20241031//EN"
        "https://jats.nlm.nih.gov/publishing/1.4/JATS-journalpublishing1-4.dtd">
<article  article-type="case-report"        dtd-version="1.4">
            <front>

                <journal-meta>
                                                                <journal-id>tjfmpc</journal-id>
            <journal-title-group>
                                                                                    <journal-title>Turkish Journal of Family Medicine and Primary Care</journal-title>
            </journal-title-group>
                                        <issn pub-type="epub">1307-2048</issn>
                                                                                            <publisher>
                    <publisher-name>Aile Hekimliği Akademisi Derneği</publisher-name>
                </publisher>
                    </journal-meta>
                <article-meta>
                                        <article-id pub-id-type="doi">10.21763/tjfmpc.610837</article-id>
                                                                <article-categories>
                                            <subj-group  xml:lang="en">
                                                            <subject>​Internal Diseases</subject>
                                                    </subj-group>
                                            <subj-group  xml:lang="tr">
                                                            <subject>İç Hastalıkları</subject>
                                                    </subj-group>
                                    </article-categories>
                                                                                                                                                        <title-group>
                                                                                                                        <article-title>A Three-Stage Assessment of a Case of Polycystic Liver Disease, Based on the Principles of Family Medicine</article-title>
                                                                                                                                        </title-group>
            
                                                    <contrib-group content-type="authors">
                                                                        <contrib contrib-type="author">
                                                                <name>
                                    <surname>Kini</surname>
                                    <given-names>Sanjay</given-names>
                                </name>
                                                                    <aff>Dept. of Community Medicine, KS Hegde Medical Academy, Deralakatte, Mangalore 575018, India.</aff>
                                                            </contrib>
                                                                                </contrib-group>
                        
                                        <pub-date pub-type="pub" iso-8601-date="20190920">
                    <day>09</day>
                    <month>20</month>
                    <year>2019</year>
                </pub-date>
                                        <volume>13</volume>
                                        <issue>3</issue>
                                        <fpage>396</fpage>
                                        <lpage>401</lpage>
                        
                        <history>
                                    <date date-type="received" iso-8601-date="20190318">
                        <day>03</day>
                        <month>18</month>
                        <year>2019</year>
                    </date>
                                                    <date date-type="accepted" iso-8601-date="20190514">
                        <day>05</day>
                        <month>14</month>
                        <year>2019</year>
                    </date>
                            </history>
                                        <permissions>
                    <copyright-statement>Copyright © 2007, Turkish Journal of Family Medicine and Primary Care</copyright-statement>
                    <copyright-year>2007</copyright-year>
                    <copyright-holder>Turkish Journal of Family Medicine and Primary Care</copyright-holder>
                </permissions>
            
                                                                                                <abstract><p>Background:Nowadays there is anincreasing trend of diagnosis of hepatic cysts due to widespread use ofultrasound examination. However, the vast majority of these cysts are benignand have an indolent course during the lifespan of the patient. Secondary toenlarging cyst size and hepatomegaly, the minority of patients develop clinicalsymptoms. Aim: Applyingthe consultation model of three-stage assessment (ie, Clinical, individual andcontextual assessment) based on the principles of family medicine, in the evaluation of a patientwith polycystic liver disease. Method: We present a case of polycystic liver disease, with clinicalmanifestations like palpable liver, shifting dullness, elevated bilirubinlevels and evaluated using three-stage-assessment model. Result: Patient had a positive attitude towards herhealth, but suffered neglect from family members. Conclusion: Positive attitude towards health anddisease, emotional support of family members, regular follow-up with theconsulting physician and genetic counseling of couples who are planning toconceive and have a family history of polycystic liver disease are some of thekey facts emphasized when we applied the three-stage-assessment model in thisparticular case.&amp;nbsp;&amp;nbsp;Giriş: Günümüzde, ultrason incelemesinin yaygınkullanımı nedeniyle hepatik kistlerin teşhisinde artış eğilimi vardır. Bununlabirlikte, bu kistlerin büyük çoğunluğu iyi huyludur ve hastanın yaşamı boyuncayavaş ilerleyen bir seyre sahiptir. Büyüyen kist büyüklüğü vehepatomegaliye&amp;nbsp; ikincil olarak, az sayıdahastada klinik semptomlar geliştirir. Amaç:Polikistik karaciğer hastalığı olan bir hastanın değerlendirilmesinde AileHekimliği İlkelerini temel alan üç aşamalı değerlendirme modelinin (örneğin;klinik, bireysel ve bağlamsal değerlendirme) uygulanması. Yöntem: Klinik olarak palpe edilebilir karaciğer, yer değiştirenmatite, artan bilirubin düzeyleri ile sunduğumuz polikistik karaciğer olgusu,üç aşamalı değerlendirme modeli kullanılarak incelendi. Bulgular: Hastanınsağlığı konusunda olumlu bir tutumu vardı, fakat aile üyeleri tarafından ihmalediliyordu. Sonuç: Üç aşamalıdeğerlendirme modelini uyguladığımız bu özel olguda; sağlık ve hastalığa karşıolumlu tutum, aile üyelerinin duygusal desteği, danışılan hekimin düzenliizlemi ve çocuk sahibi olmayı planlayan ve ailede polikistik karaciğerhastalığı öyküsü olan çiftlerin genetik danışmanlığı kilit noktalar olarakvurgulanmıştır.</p></abstract>
                                                                                    
            
                                                            <kwd-group>
                                                    <kwd>Polycystic liver disease</kwd>
                                                    <kwd>  three stage assessment</kwd>
                                                    <kwd>  family medicine</kwd>
                                            </kwd-group>
                                                        
                                                                                                                                                    </article-meta>
    </front>
    <back>
                            <ref-list>
                                    <ref id="ref1">
                        <label>1</label>
                        <mixed-citation publication-type="journal">1.	Bistritz L, Tamboli C, Bigam D, Bain VG: Polycystic liver disease: experience at a teaching hospital. Am J Gastroenterol 2005, 100(10):2212-2217.</mixed-citation>
                    </ref>
                                    <ref id="ref2">
                        <label>2</label>
                        <mixed-citation publication-type="journal">2.	Turnage RH, Eckhauser FE, Knol JA, Thompson : Therapeutic dilemmas in patients with symptomatic polycystic liver disease. Am Surg 1988, 54(6):365-372.</mixed-citation>
                    </ref>
                                    <ref id="ref3">
                        <label>3</label>
                        <mixed-citation publication-type="journal">3.	Russell RT, Pinson CW: Surgical management of polycystic liver disease. World J Gastroenterol 2007, 13(38):5052-5059.</mixed-citation>
                    </ref>
                                    <ref id="ref4">
                        <label>4</label>
                        <mixed-citation publication-type="journal">4.	Van Erpecum KJ, Janssens AR, Terpstra JL, Tjon A, Tham RJ: Highly symptomatic adult polycystic disease of the liver. A report of fifteen cases. J Hepatol 1987, 5(1):109-117.</mixed-citation>
                    </ref>
                                    <ref id="ref5">
                        <label>5</label>
                        <mixed-citation publication-type="journal">5.	Woolnough et al.: Polycystic liver disease presenting with an exudative pleural effusion: a case report. Journal of Medical Case Reports 2012 6:107.</mixed-citation>
                    </ref>
                                    <ref id="ref6">
                        <label>6</label>
                        <mixed-citation publication-type="journal">6.	Salustio R, Ribeiro JV. Polycystic liver disease. BMJ Case Rep 2014; 1-3</mixed-citation>
                    </ref>
                                    <ref id="ref7">
                        <label>7</label>
                        <mixed-citation publication-type="journal">7.	Arnold HL, Harrisson SA: New advances in evaluation and management of patients with polycystic liver disease. Am J Gastroenterol 2005, 100(11):2569-2582</mixed-citation>
                    </ref>
                                    <ref id="ref8">
                        <label>8</label>
                        <mixed-citation publication-type="journal">8.	Doctor-Patient Communication: A Review. Jennifer Fong Ha, and Nancy Longnecker, Ochsner J. 2010 Spring; 10(1): 38–43 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096184/</mixed-citation>
                    </ref>
                                    <ref id="ref9">
                        <label>9</label>
                        <mixed-citation publication-type="journal">9.	Fehrsen GS and Henbest RJ. In Search of Excellence. Expanding the patient-centred clinical method: a three-stage assessment. Family Practice 1993; 10-49-54.</mixed-citation>
                    </ref>
                            </ref-list>
                    </back>
    </article>
