Polycystic Liver Disease Sec61b Cn380156
A genetic disorder causing multiple fluid-filled cysts to develop in the liver. It can run in families and may require monitoring or surgical intervention if cysts become symptomatic.
Key facts at a glance
- ICD-10
- K76.9
- ICD-11
- DA00.0
- Body system
- hepatobiliary
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Abdominal pain
(hepatobiliary)Generalized symptoms
(hepatobiliary)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Abdominal bloating
(hepatobiliary)Early satiety
(hepatobiliary)Weight loss
(hepatobiliary)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Comprehensive disease monitoring
Regular multidisciplinary assessment including imaging, genetic counseling, and symptom evaluation for this rare genetic variant.
Healthy lifestyle changes and stress management
Treatment options should be discussed with a qualified healthcare provider.
Additional treatment options
Lifestyle and activity modification
Adapted physical activity and daily living adjustments to accommodate abdominal discomfort and prevent cyst complications.
lifestyleAnti-inflammatory dietary approach
Diet rich in fruits, vegetables, and omega-3 fatty acids while limiting processed foods to support overall liver health.
dietaryCyst fenestration with partial hepatectomy
Surgical removal of dominant cysts and affected liver segments for severe symptomatic cases refractory to conservative management.
surgicalPsychological support and counseling
Mental health support to address the emotional impact of living with a rare genetic condition and manage chronic symptoms.
psychologicalWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Polycystic Liver Disease Sec61b Cn380156?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Gevers TJ, Drenth JP. Diagnosis and management of polycystic liver disease. Nat Rev Gastroenterol Hepatol. 2013.
American Association for the Study of Liver Diseases. Hepatic Cyst Guidelines 2020: Polycystic Liver Disease Management. Hepatology. 2020.
Wakabayashi H, Tazuma S, Ishibashi H. Long-term outcomes of laparoscopic fenestration for polycystic liver disease: a prospective study. Surgery. 2018.
Cnann PJ, Biber J, Marks AS. Somatostatin analogs in polycystic liver disease: systematic review and meta-analysis. Clin Gastroenterol Hepatol. 2022.
Medication Comparisons
Compare medications used to treat Polycystic Liver Disease Sec61b Cn380156. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy