GRANULOMATOUS LIVER DISEASE
Hepatic granulomas are common, being found in 2 to 10 per cent of all liver biopsies, often in association with an elevated serum alkaline phosphatase level. However, they are rarely a specific finding and have been reported in association with a wide variety of infections, systemic illnesses, hepatobiliary disorders, drugs, and toxins, some of which are listed in. Although granulomas are a nonspecific finding, occasionally specific features are seen, such as acidfast bacilli in tuberculosis, ova in schistosomiasis, larvae in toxocariasis, and birefringent granules in starch, talc, or silicone granulomas. The differential diagnosis of hepatic granulomas is one of the most extensive in medicine, and the workup requires meticulous attention to details of the history, physical examination, and laboratory tests. Indeed, in 20 per cent or more of patients, no cause for granulomas is found despite extensive investigation. A subset of these patients, who have a syndrome consisting of fever, hepatomegaly, and hepatic granulomas which responds to administration of corticosteroids, has been described as having granulomatous hepatitis, although some feel that these individuals have a variant of sarcoidosis.
Conversely, liver biopsy (and culture, particularly of acidfast bacteria) is of considerable value in the diagnosis of sarcoidosis, miliary tuberculosis, and histoplasmosis, as virtually all patients with these disorders will have hepatic granulomas. Similarly, characteristic granulomas are seen in many patients with primary biliary cirrhosis, and granulomas may be the first clue to Hodgkin’s disease.
- Improving Case Management
- LIVER ABSCESS
- Endocrine Systems
- CLINICAL MANIFESTATIONS OF ENDSTAGE RENAL DISEASE
- Conjugated Hyperbilirubinemia
- THE COMMON CLINICAL MANIFESTATIONS OF GASTROINTESTINAL DISEASE
- GENERAL SURGERY IN THE PATIENT WITH HEART DISEASE
- Hematuria
- Studies of Pancreatic Structure and Function
- Women’s Health Program
- PATHOPHYSIOLOGY OF AIRWAY OBSTRUCTION
- Screening and Prevention
- MYOCARDIAL METABOLISM
- Therapy
- CARCINOMA OF THE PANCREAS - Clinical Manifestations
- Direct (Toxic Nephropathy)
- Polycystic Kidney Disease (PKD)
- Renal Tubular Acidosis
- Blood Chemistries
- CYSTIC FIBROSIS
- Liddle’s Syndrome
- THE FAMILIAL POLYPOSIS SYNDROMES
- Other Clearly Extrinsic Causes of Diffuse Infiltrative Lung Disease
- DRUGS
- AORTIC ARTERITIS
- PHYSICAL EXAMINATION
- Renal Artery Occlusion
- EFFECTORS OF THE RESPIRATORY SYSTEM
- POLYPS OF THE GASTROINTESTINAL TRACT
- Bartter’s Syndrome
- Sickle Cell Anemia (SS)
- CLINICAL CLASSIFICATION OF JAUNDICE
- Genitourinary System
- CLINICAL APPROACH TO LIVER DISEASE
- PHYSIOLOGY OF THE PULMONARY CIRCULATION