Diagnosis and Treatment of Crusted Scaly Scalp and Leg Lesions in a Patient with Liver Disease and Arsenic Exposure
Primary Diagnosis
The most likely diagnosis is arsenical keratosis with underlying chronic arsenic-induced liver disease, requiring immediate cessation of arsenic exposure, dermatologic management of skin lesions, and hepatologic evaluation for potential cirrhosis or portal hypertension. 1, 2
Differential Diagnosis to Consider
Arsenical Skin Changes (Most Likely)
- Chronic arsenic ingestion causes characteristic crusted, scaly skin lesions (arsenical keratoses) that typically appear on palms, soles, and can occur on scalp and extremities 1
- These lesions are well-documented in patients with chronic arsenicosis and often accompany liver disease 1, 2
- The combination of liver disease history with crusted scaly lesions strongly suggests chronic arsenic toxicity 1
Psoriasis (Alternative Consideration)
- Thick psoriatic plaques can present as crusted scaly lesions on scalp and extremities 3
- However, psoriasis typically presents with hundreds of lesions involving larger body surface area (not just scalp and one leg lesion) 3
- The presence of liver disease and arsenic exposure makes arsenical keratosis more likely 1
Erosive Pustular Dermatosis of Scalp (Less Likely)
- This condition presents with pustular lesions, erosions, and crusts on scalp in elderly patients 4
- Autoimmune hepatitis is an associated condition with erosive pustular dermatosis 4
- However, this typically affects only the scalp and is not associated with leg lesions 4
Critical Diagnostic Workup
Immediate Skin Assessment
- Examine for additional arsenical skin changes including hyperpigmentation, palmar/plantar keratoses, and Bowen's disease (intraepithelmal carcinoma) 1
- Document distribution and characteristics of all skin lesions
- Consider skin biopsy if diagnosis remains uncertain, though arsenical keratoses have characteristic clinical appearance 1
Arsenic Exposure Confirmation
- Obtain detailed history of water source, occupational exposures, and traditional medicine use 2
- Measure 24-hour urinary arsenic levels (elevated >50 μg/L suggests chronic exposure) 2
- Consider hair and nail analysis for chronic exposure assessment 1
Hepatic Evaluation (Critical Given Liver Disease History)
- Hepatomegaly is present in 76.6% of patients with chronic arsenicosis 2
- Noncirrhotic portal fibrosis is the predominant lesion (91.3% of cases) in arsenic-induced liver disease 2
- Obtain complete liver function tests including AST, ALT, alkaline phosphatase, bilirubin, albumin, and globulin 5, 2
- Check for elevated globulin levels, which occur in chronic arsenicosis 2
- Perform abdominal ultrasound to assess for hepatomegaly, splenomegaly, portal hypertension, and exclude hepatocellular carcinoma 3
- Screen for esophageal varices with upper endoscopy if portal hypertension is suspected 3, 2
Malignancy Screening (Essential)
- Chronic arsenic exposure increases risk of hepatocellular carcinoma, even in non-cirrhotic livers 1
- Measure serum alpha-fetoprotein (AFP) to screen for HCC 3
- Perform multiphasic contrast-enhanced CT or MRI if any liver mass is detected or AFP is elevated 6
- Arsenical keratoses can transform into squamous cell carcinoma or Bowen's disease 1
Exclude Competing Diagnoses
- Rule out viral hepatitis (HBsAg, anti-HCV) as these can coexist with arsenic toxicity 2
- Consider autoimmune hepatitis if ANA positive and transaminases markedly elevated 7
- Exclude Wilson's disease if patient is young (<40 years) with unexplained liver disease 3
Treatment Algorithm
Immediate Interventions
Step 1: Eliminate Arsenic Exposure
- Identify and remove source of arsenic exposure immediately 1, 2
- Provide arsenic-free water supply 2
- This is the single most important intervention to prevent disease progression 2
Step 2: Hepatoprotective Therapy
- Consider N-acetylcysteine (NAC) supplementation, which has been shown to abrogate arsenic-induced liver injury through glutathione-dependent mechanisms 8
- NAC prevents mitochondrial oxidative stress and apoptotic liver cell death in arsenic toxicity 8
Step 3: Dermatologic Management
- For arsenical keratoses: topical keratolytics (salicylic acid, urea preparations)
- Monitor closely for malignant transformation to squamous cell carcinoma 1
- If lesions are suspicious for malignancy, perform biopsy 1
Management of Liver Disease Complications
Portal Hypertension Management
- If esophageal varices develop, initiate non-selective beta-blockers for primary prophylaxis 3
- Monitor for ascites, hepatic encephalopathy, and variceal bleeding 3, 5
Hepatocellular Carcinoma Surveillance
- Perform abdominal ultrasound every 6 months for HCC surveillance 3
- Patients with arsenic-induced liver disease require lifelong HCC surveillance even without cirrhosis 1
Liver Transplantation Consideration
- If patient develops decompensated cirrhosis or HCC within Milan criteria, refer for liver transplantation evaluation 3
- Arsenic-induced liver disease is a valid indication for transplantation 3
Long-Term Monitoring
Follow-Up Schedule
- Cohort studies show that even after switching to arsenic-free water, patients can develop esophageal varices and elevated globulin over 2-12 years 2
- Monitor liver function tests every 3-6 months indefinitely 2
- Continue HCC surveillance with ultrasound ± AFP every 6 months 3
- Annual dermatologic examination for skin cancer screening 1
Critical Pitfalls to Avoid
- Do not assume liver disease is "cryptogenic" without investigating arsenic exposure history 1
- Do not discontinue HCC surveillance even if liver function normalizes, as HCC can develop in non-cirrhotic arsenic-exposed livers 1
- Do not ignore single skin lesions as benign—arsenical keratoses require close monitoring for malignant transformation 1
- Do not delay removal of arsenic source while awaiting confirmatory testing 2
- Do not assume disease will resolve completely after arsenic cessation—portal hypertension can progress despite removal of exposure 2