{"id":2068,"date":"2020-09-15T11:10:30","date_gmt":"2020-09-15T11:10:30","guid":{"rendered":"http:\/\/hjog.org\/?p=2068"},"modified":"2022-02-03T10:11:40","modified_gmt":"2022-02-03T10:11:40","slug":"case-reportwilsons-disease-in-pregnancy-presentation-of-a-case-report","status":"publish","type":"post","link":"https:\/\/hjog.org\/?p=2068","title":{"rendered":"Wilson`s disease in pregnancy: presentation of a case report."},"content":{"rendered":"

Case Report<\/span><\/p>\n

Ioannis Thanopoulos, Kalliopi Pappa<\/p>\n

1st<\/sup> department of Obstetrics and Gynecology, Alexandra Hospital, National and Kapodistrian University of Athens, Greece.<\/p>\n

Correspondence:\u00a0<\/em>Kalliopi Pappa, 2-4 Lourou str, 11528, Athens, Greece, Email: kpappa@med.uoa.gr<\/a><\/p>\n

\"\"<\/a><\/p>\n

 <\/p>\n

\n
Abstract<\/strong><\/h5>\n

Wilson\u2019s disease is a rare inherited autosomal recessive disorder of copper metabolism causing toxic hepatic and neural accumulation. The gene that regulates the disease is located on chromosome 13 (13q14.3). The signs and symptoms of Wilson\u2019s disease vary depending on the organs that are affected by the disease with almost all the patients showing evidence of progressive liver disease. Its severity varies and is strongly associated with the time of diagnosis. In the present case report we present a rare case presenting with Wilson`s disease during pregnancy and review current management options.<\/p>\n

Introduction<\/strong><\/h5>\n

Wilson\u2019s disease is a rare inherited autosomal recessive disorder of copper metabolism causing toxic hepatic and neural accumulation. The disease gene (ATP7B<\/em>) is located on\u00a0chromosome 13\u00a0(13q14.3). The signs and symptoms of Wilson\u2019s disease vary depending on the organs that are affected by the disease with almost all the patients showing evidence of progressive liver disease. The disease presents a wide spectrum of clinical manifestations from asymptomatic to chronic liver disease or liver failure. The most common symptoms are neuropsychiatric problems.1<\/sup> The severity of disease vary and is strongly associated with the time of diagnosis. However the disease can be managed and the early diagnosis and treatment of asymptomatic patients keep away from the development of symptoms. Wilson\u2019s disease can be fatal if not recognized and treated in advanced stages when it is symptomatic. The current treatments include zinc salts and chelating agents (D-penicillamine and trientine).2<\/sup><\/p>\n

Regarding pregnancy, prior to introduction of penicillamine Wilson\u2019s disease had been linked to subfertility due to menstrual irregularities and the early onset of chronic liver disease. In cases where pregnancy occurred it mostly resulted in spontaneous miscarriage. Therapeutic evolution resulted in successful pregnancy outcomes. Maintenance of medical treatment during pregnancy is recommended while patients are usually monitored closely for hepatic and neuropsychiatric symptoms. Anti-copper therapy during pregnancy is found to be safe.3<\/sup><\/p>\n

Case Presentation<\/strong><\/h5>\n

A 27 year old pregnant woman, G1P0 , with a history of Wilson\u2019s disease was referred to the Maternal Unit of Alexandra Athens University Hospital during the third trimester of her spontaneous pregnancy (at 34w4d of gestation) for a gastroenterological assessment and a caesarian section booking appointment due to her choice to give birth with caesarian.<\/p>\n

The patient had dyslipidemia which was well controlled with diet; she had no allergies or gynaecological problems. The liver function and blood clotting tests (INR, PT, aPPT) were regularly checked during gestation and were within the normal range. All the antenatal laboratory tests and fetal scans were within normal limits.<\/p>\n

Regarding patient\u2019s family history, her parents were both diagnosed with Wilson\u2019s disease as well as her older sister. The patient\u2019s sister died three months after her first baby\u2019s delivery suffering from cirrhosis and liver carcinoma, which was attributed to poor treatment compliance.<\/p>\n

During pregnancy, patient was under treatment with penicillamine 250 mg daily and zinc 50mg twice a day. Her pregnancy remained uncomplicated and uneventful until the end. At 37w3d of gestation the patient underwent caesarean delivery of a healthy girl weighing 3.060 kg with a good Apgar score (8 in the first minute). The patient was discharged on the 4th<\/sup> postnatal day.<\/p>\n

Discussion<\/strong><\/h5>\n

Wilson disease affects many organs and systems. Starting from liver, it causes hepatic failure and cirrhosis, neurological symptoms as tremors and dyskinesias, phychiatric disorders like depression, anxiety and phychosis, kayser-fleishcer ring around limbus and renal tubular damage leading to chronic hypertention. It impaires the female reproductive system causing menstrual irregularities and miscarriagies \u00a0from copper deposition in uterus. It can also cause thrombocytopenia, leukopenia and haemolytic anaemia. Also cardiac arrythmia, cardiomyopathy , myopathy, osteoporosis and chondrocalcinosis can occur.4<\/sup><\/p>\n

During pregnancy the levels of serum copper and ceruloplasmin should be measured every trimester as they peak around 24th<\/sup> week of pregnancy and then follow a plateau.<\/p>\n

Untreated cases usually lead to miscarriages probably because of highly copper concentration in uterus. Use of penicilamine and zinc is considered safe in pregnancy and improves the outcome for mother and fetus. Zinc interferes with copper\u2019s absorption through intestinal metallothionein cells and penicilamine lead to an increase in copper excretion from urine.<\/p>\n

As Wilson disease can cause chronic hypertention due to kidney damage, it may lead to hypertention of pregnancy or preeclampsia too, although these morbidities can be independently developed.5<\/sup><\/p>\n

Conclusion<\/strong><\/h5>\n

Patients with Wilson\u2019s disease receiving regular treatment before gestation are usually able to conceive spontaneously and have a successful pregnancy with a good outcome. Use of Zinc Sulphate and penicilamine during pregnancy is safe and with good results. However, since Wilson\u2019s disease is associated with miscarriages and pregnancy hypertension\/preeclampsia, these pregnant should be considered and managed as high risk.6<\/sup> In our case the pregnancy had no complications and the blood pressure was well controlled during gestation.<\/p>\n

References<\/strong><\/h5>\n

1. Mohr, I., & Weiss, K. H. Biochemical Markers for the Diagnosis and Monitoring of Wilson Disease. Clin Biochem Rev. 2019; 40: 59\u201377.
\n2. Kanitkar, M., JOSHi, S. N., & Roy, N. D. WILSON’S DISEASE (A report of two cases). Med J Armed Forces India. 1994; 50: 63\u20135.
\n3. Pfeiffenberger J, Beinhardt S, et al. Pregnancy in Wilson’s disease: Management and outcome. Hepatology. 2018 Apr;67:1261-9.
\n4. Merle, U., Schaefer, M., Ferenci, P., & Stremmel, W. Clinical presentation, diagnosis and long-term outcome of Wilson’s disease: a cohort study. Gut, 2007;56:115-20.
\n5. Malik, A., Khawaja, A., & Sheikh, L. Wilson’s disease in pregnancy: case series and review of literature. BMC Res Notes. 2013; 6: 421.
\n6.Nunns, D., Hawthorne, B., Goulding, P., Maresh, M. Wilson’s disease in pregnancy case report. Eur J Obstet Gynecol Reprod Biol. 1995;62:141-3.<\/p>\n","protected":false},"excerpt":{"rendered":"

Ioannis Thanopoulos, Kalliopi Pappa<\/p>\n

\"\"<\/a><\/p>\n

 <\/p>\n

 
\nWilson\u2019s disease is a rare inherited autosomal recessive disorder of copper metabolism causing toxic hepatic and neural accumulation. The gene that regulates the disease is located on chromosome 13 (13q14.3). The signs and symptoms of Wilson\u2019s disease vary depending on the organs that are affected by the disease with almost all the patients showing evidence of progressive liver disease. Its severity varies and is strongly associated with the time of diagnosis. In the present case report we present a rare case presenting…
\n“> Read More…<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[912],"tags":[],"class_list":["post-2068","post","type-post","status-publish","format-standard","hentry","category-2020-volume-19-issue-3"],"_links":{"self":[{"href":"https:\/\/hjog.org\/index.php?rest_route=\/wp\/v2\/posts\/2068","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/hjog.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/hjog.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/hjog.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/hjog.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=2068"}],"version-history":[{"count":3,"href":"https:\/\/hjog.org\/index.php?rest_route=\/wp\/v2\/posts\/2068\/revisions"}],"predecessor-version":[{"id":2665,"href":"https:\/\/hjog.org\/index.php?rest_route=\/wp\/v2\/posts\/2068\/revisions\/2665"}],"wp:attachment":[{"href":"https:\/\/hjog.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=2068"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/hjog.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=2068"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/hjog.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=2068"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}