Signs and Symptoms of Primary Hyperparathyroidism

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Below is your **complete, expanded, exam-ready + clinically robust reference** on **Primary Hyperparathyroidism (PHPT)** following **your template**: **Definition → Pathophysiology → Causes → Clinical Features → Investigations → Differential Diagnosis → Management (stepwise) → Drug details → Monitoring → Counselling** — **Concise but exhaustive**, suitable for NEET PG + physicians + your ErrorOn Space content. --- # **PRIMARY HYPERPARATHYROIDISM (PHPT) – COMPLETE DETAILED NOTE** --- # **1) Definition** Primary hyperparathyroidism is a disorder characterized by **autonomous overproduction of parathyroid hormone (PTH)** from one or more parathyroid glands, leading to **hypercalcemia** and **hypophosphatemia** with widespread metabolic, renal, skeletal, and neuropsychiatric effects. --- # **2) Pathophysiology** Excess PTH causes: ### **A. Bone** * ↑ Osteoclast activity * ↑ Bone resorption * Cortical bone loss (radius most affected) * Osteitis fibrosa cystica (late) ### **B. Kidneys** * ↑ Calcium reabsorption * ↓ Phosphate reabsorption → **hypophosphatemia** * ↑ 1α-hydroxylase → ↑ 1,25-(OH)₂-Vitamin D → ↑ gut calcium absorption * Nephrolithiasis and nephrocalcinosis ### **C. GI** * ↑ Gastrin → peptic ulcer * ↑ Calcium absorption ### **D. Cardiovascular** * Short QT interval * Hypertension * Arrhythmias (rare) --- # **3) Etiology (Causes)** ### **A. Parathyroid Adenoma (80–85%)** Single adenoma most common. ### **B. Parathyroid Hyperplasia (10–15%)** All four glands enlarged. ### **C. Parathyroid Carcinoma (<1%)** Severe hypercalcemia, palpable neck mass. ### **D. Genetic Syndromes** * MEN 1 * MEN 2A * Familial isolated hyperparathyroidism * Familial hypocalciuric hypercalcemia (FHH) – mimics PHPT but NOT PHPT ### **E. Radiation Exposure** Childhood neck radiation increases risk. --- # **4) Clinical Features** Mnemonic: **“Stones, Bones, Groans, Thrones, Psychiatric Overtones”** ### **A. Renal** * Nephrolithiasis * Nephrocalcinosis * Polyuria, polydipsia * Dehydration * CKD ### **B. Skeletal** * Bone pain * Cortical osteoporosis * Pathological fractures * Brown tumors * Subperiosteal erosions ### **C. GI** * Nausea, vomiting * Constipation * Pancreatitis * Peptic ulcer disease * Abdominal pain ### **D. Neuropsychiatric** * Fatigue * Depression * Cognitive dysfunction * Confusion (hypercalcemic crisis) ### **E. Cardiovascular** * Hypertension * Short QT interval ### **F. Musculoskeletal** * Proximal myopathy * Generalized weakness ### **G. Others** * Corneal calcification (band keratopathy) --- # **5) Investigations (Stepwise)** ## **A. Initial Tests** | Test | Typical Finding in PHPT | | --------------------- | ------------------------ | | **Serum calcium** | ↑↑ (total & ionized) | | **Serum PTH** | **Inappropriately high** | | **Serum phosphate** | ↓ | | **Vitamin D (25-OH)** | Low/normal | | **Renal function** | Normal or ↓ | --- ## **B. Confirmatory Tests** ### **1) 24-hr Urinary Calcium** * **High or normal** in PHPT * **Low** in FHH → **key differentiator** ### **2) Imaging (for localization, NOT diagnosis)** * **Sestamibi Tc-99m scan** (best for adenoma) * Ultrasound neck * 4D CT (pre-operative planning) ### **3) Bone Density (DEXA)** * Low BMD, especially cortical bone (radius) --- # **6) Differential Diagnosis** | Condition | Differentiating Features | | ---------------------------------------------- | ----------------------------------------- | | **FHH (Familial Hypocalciuric Hypercalcemia)** | Low urinary calcium (<100 mg/day), benign | | **Tertiary hyperparathyroidism** | CKD history, very high PTH | | **Malignancy-associated hypercalcemia** | Low PTH, high PTHrP | | Vitamin D intoxication | High Ca + high phosphate | | Sarcoidosis | High Ca + high Vit D | | Thyrotoxicosis | Mild hypercalcemia, high T3/T4 | --- # **7) Management (Stepwise)** ## **A. Indications for Parathyroidectomy (Definitive Treatment)** (As per **Fourth International Workshop** & clinical guidelines) Surgery **recommended** when ANY of the following are present: 1. Serum calcium **>1.0 mg/dL above upper normal** 2. Age **<50 years** 3. Creatinine clearance **<60 mL/min** 4. Nephrolithiasis or nephrocalcinosis 5. Hypercalciuria (>400 mg/24 hours) 6. T-score ≤ −2.5 at any site 7. Fragility fracture 8. Vertebral compression fracture --- ## **B. Surgical Options** * Minimally invasive parathyroidectomy (single adenoma) * Bilateral neck exploration (hyperplasia) * Total parathyroidectomy + autotransplantation (selected cases) --- ## **C. Medical Management (when not surgical candidate)** ### **1) Cinacalcet** **Indication:** * Severe hypercalcemia when surgery not possible * Parathyroid carcinoma * Persistent disease post-surgery **Mechanism:** Calcimimetic → increases CaSR sensitivity → ↓ PTH secretion. **Dose:** * Start **30 mg twice daily**, titrate to calcium levels. **Side effects:** * Nausea, vomiting * Hypocalcemia * QT prolongation (rare) **Monitoring:** * Calcium levels 1 week after dose change * PTH every 3–6 months --- ### **2) Bisphosphonates** (Alendronate / Zoledronic acid) **Indication:** * Osteoporosis due to PHPT **Mechanism:** Inhibit osteoclast-mediated bone resorption. **Dose:** * **Alendronate 70 mg weekly** * **Zoledronic acid 5 mg IV yearly** **Side effects:** * Esophagitis (PO) * Acute-phase reaction (IV) * Hypocalcemia (rare) **Monitoring:** * BMD yearly * Calcium before each IV dose --- ### **3) Vitamin D Replacement** Correct deficiency to prevent worsening PTH: * **Cholecalciferol 1000–2000 IU/day** * Target 25-OH Vit D > 30 ng/mL **Important:** Correct slowly to avoid raising Ca too much. --- ### **4) Hydration + Lifestyle** * Drink ≥2.5–3L/day * Avoid thiazides * Avoid high-dose calcium supplements * Weight-bearing exercise * Avoid prolonged immobilization --- ## **D. Hypercalcemic Crisis – Emergency** **Severe Ca >14 mg/dL** Immediate steps: 1. **IV normal saline** 2. **IV furosemide** (after hydration) 3. **IV calcitonin** 4. **IV bisphosphonate (zoledronic acid)** 5. Dialysis if renal failure --- # **8) Complications** * CKD * Severe osteoporosis * Pathological fractures * Pancreatitis * Peptic ulcer * Parathyroid carcinoma (rare) * Cardiac arrhythmias * Hypercalcemic crisis --- # **9) Monitoring After Treatment** ### **If Surgery Done** * Serum calcium at 24 hours * PTH within 6 months * DEXA every 12–24 months ### **If Managed Medically** * Serum calcium every 6 months * PTH every 6–12 months * Vitamin D yearly * DEXA every 1–2 years * Renal ultrasound yearly --- # **10) Patient Counselling Points** * Stay well hydrated * Avoid thiazide diuretics * Avoid prolonged immobilization * Maintain Vit D in normal range * Watch for symptoms of hypercalcemia: * Polydipsia * Polyuria * Fatigue * Constipation * Explain that **surgery is curative** in most cases (95–98%) --- # **11) Tags (comma separated)** Primary Hyperparathyroidism, Hypercalcemia, PTH, Parathyroid Adenoma, Parathyroidectomy, Stones Bones Groans, Osteitis Fibrosa Cystica, Hyperparathyroid Crisis, Cinacalcet, Nephrolithiasis, Endocrinology, NEET PG Notes, ErrorOn Space Medical Notes --- If you want, I can now generate: ✅ **Case scenarios (10, 20, or 35 as needed)** ✅ **Hard MCQs with explanations** ✅ **HTML/PHP formatted version for your website** ✅ **Structured JSON meta (title, tags, slug, meta description)** Just tell me!

Tags: Primary Hyperparathyroidism PHPT Hypercalcemia Parathyroid Adenoma Parathyroid Hyperplasia Parathyroid Carcinoma PTH Excess Stones Bones Groans Renal Stones Nephrolithiasis Nephrocalcinosis Osteitis Fibrosa Cystica Bone Resorption Hypercalciuria Hypophosphatemia Sestamibi Scan Parathyroidectomy Cinacalcet Bisphosphonates Endocrinology Calcium Metabolism Disorders Parathyroid Disorders Metabolic Bone Disease NEET PG Endocrinology ErrorOn Space Medical Notes
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