Add comprehensive documentation for adrenal conditions

- Created detailed articles for Adrenal Adenoma, Adrenal Cyst, Adrenal Myelolipoma, and general Adrenal anatomy.
- Included key facts, imaging findings, differential diagnoses, pathology, clinical issues, and diagnostic checklists for each condition.
- Enhanced understanding of adrenal tumors and their characteristics through structured documentation.
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---
title: "Adrenal Cyst"
docid: "c5d717a3-3d6e-4e86-9efe-1ad0ec14740f"
breadcrumbs:
- "Genitourinary"
- "Diagnosis"
- "Adrenal"
- "Benign Neoplasms"
- "Adrenal Cyst"
---
# KEY FACTS
- ## Imaging
- "Adrenal cyst" is descriptive term, not pathological diagnosis
- True adrenal cysts
- Majority are endothelial cysts (lymphangiomas)
- Epithelial cysts exceedingly rare
- Simple, or minimally complex, adrenal cyst, thin rim calcification, no enhancement
- Pseudocysts
- Prior hemorrhage inferred
- Nonenhancing but complex contents and wall calcification
- Relevant history (extraadrenal malignancy, rapid growth), biochemical evaluation (cortisol, metanephrines): Consider underlying adrenal neoplasm
- Enhancing soft tissue components may suggest adrenal mass hemorrhage and pseudocyst formation
- Parasitic (echinococcal) cyst
- Rare outside endemic areas
- Typically in setting of generalized echinococcus
- ## Top Differential Diagnoses
- Adrenal adenoma
- CECT: Enhancing mass without visible wall or peripheral calcifications
- Gastric diverticulum
- Air-, fluid-, or contrast-filled mass with no enhancement of contents
- Adrenal myelolipoma
- Macroscopic fat
- Necrotic adrenal tumor
- Complex wall with heterogeneous contents
- Retroperitoneal bronchogenic cyst
- ## Clinical Issues
- No treatment required usually
- Imaging surveillance performed, although intensity and length of follow-up not defined
- Biochemical evaluation (cortisol, metanephrines) routinely performed to exclude underlying adrenal neoplasm
- Surgical resection for complex cyst with enhancing components, or symptomatic cyst
- ## Diagnostic Checklist
- Complicated cyst has high attenuation, thick enhancing wall, &/or septations
# TERMINOLOGY
- ## Definitions
- "Adrenal cyst" is descriptive term, not pathological diagnosis
- Can mean true cyst, pseudocyst, or cystic mass
# IMAGING
- ## General Features
- ### Best diagnostic clue
- Well-defined, nonenhancing, water-density adrenal mass ± calcifications
- ### Location
- Suprarenal
- Unilateral > bilateral (8-10% of cases)
- ### Size
- < 5 cm (50%), up to 20 cm
- ## CT Findings
- ### NECT
- Unilocular or multilocular mass
- Well-defined, round to oval, homogeneous mass usually with water (0 HU) or near-water density
- Higher- or mixed-attenuation mass (hemorrhage, intracystic debris, crystals)
- Wall usually very thin
- ↑ wall thickness, up to 3 mm for complex cysts
- Calcifications
- Rim-like or nodular (51-69%)
- Centrally in intracystic septation (19%)
- Punctate within intracystic hemorrhage (5%)
- ### CECT
- No central enhancement ± wall enhancement
- Coronal reformats helpful to determine organ of origin if large cyst
- ## MR Findings
- ### T1WI
- Homogeneous, hypointense mass
- Hyperintense mass (hemorrhage)
- ### T2WI
- Hyperintense mass
- ## Ultrasonographic Findings
- Simple or septated suprarenal cyst
- Shadowing from calcification
- Real-time examination helpful to differentiate adrenal cyst from adjacent (renal, pancreatic) cyst
- ## Imaging Recommendations
- ### Best imaging tool
- CECT or MR; US for confirmation
# DIFFERENTIAL DIAGNOSIS
- [Adrenal Adenoma](/document/adrenal-adenoma/e2916d86-5f9f-4dd3-9576-1a7b89d8dda0)
- NECT: Lipid-rich adenoma (< 10 HU) mimics adrenal cyst
- Peripheral or septal calcification favors adrenal cyst
- CECT: **Enhancing mass** without visible wall or peripheral calcifications
- Assess washout kinetics to diagnose lipid-poor adenoma
- MR: Signal suppression at out-of-phase, chemical-shift imaging
- US: Solid adrenal lesion
- [Gastric Diverticulum](/document/gastric-diverticulum/eeb101f0-8bdf-4771-b44a-fe6e73b3a463)
- May simulate left adrenal cyst
- Air-, fluid-, or contrast-filled suprarenal mass
- No enhancement
- Normal adjacent adrenal gland
- [Adrenal Myelolipoma](/document/adrenal-myelolipoma/5813a554-06a4-4696-af71-7ce50693039d)
- Fat (not fluid) attenuation mass
- ## Necrotic Adrenal Tumor
- Primary (pheochromocytoma or carcinoma) or metastatic
- Clinical history, biochemical evaluation, lesion complexity suggest correct diagnosis
- Enhancing soft tissue components
- ## Retroperitoneal Bronchogenic Cyst
- Rare, benign, suprarenal fluid or soft tissue attenuation lesion
- Adjacent to but separate from adrenal gland
- ## Renal Cyst
- Coronal MR/CT or US useful to determine organ of origin of large, retroperitoneal cystic lesions
# PATHOLOGY
- ## General Features
- ### Etiology
- Congenital (endothelial, epithelial) cysts
- Acquired (post hemorrhagic, inflammatory) pseudocysts
- Cystic, hemorrhagic degeneration of underlying adrenal neoplasm
- ## Staging, Grading, & Classification
- Accepted classification scheme
- Pseudocyst
- Most common type of cystic adrenal lesion in surgical series
- No epithelial or endothelial lining: Fibrous cyst wall
- Potentially as complication of prior trauma or hemorrhage though history of such often not elicited
- May be associated with underlying adrenal neoplasm (pheochromocytoma, adrenal carcinoma, myelolipoma)
- Attenuation and complexity at imaging varies depending upon hemorrhagic component
- Wall and septal calcification common
- Endothelial cyst
- Subtypes: Lymphangiomatous and hemangiomatous
- True cyst: Endothelial lining
- Originate from preexisting vascular malformation or obstructed, ectatic lymphatic channels
- Thin rim calcification typical
- Epithelial cyst
- Extremely rare: No acinar structures within normal adrenal gland
- Mesothelial origin suggested (mesothelial cells potentially incorporated within adrenal gland during embryogenesis)
- Parasitic (hydatid) cyst
# CLINICAL ISSUES
- ## Presentation
- ### Most common signs/symptoms
- Typically asymptomatic
- Larger cysts may be symptomatic
- Abdominal pain
- Hemorrhage
- Clinical history (malignancy, hypertension) elicited
- May indicate cystic degeneration of underlying adrenal neoplasm (e.g., metastasis, pheochromocytoma)
- Diagnosis
- Usually incidental finding at imaging
- Endocrine-biochemical evaluation performed to exclude underlying functional adrenal tumor
- ## Demographics
- ### Age
- Any, though patients 20-50 years of age most common
- ### Sex
- M:F = 1:3
- ### Epidemiology
- Uncommon entity: Autopsy incidence 0.064-0.18%
- Accounts for 1% of incidental adrenal lesions in large imaging series
- ## Natural History & Prognosis
- Complications
- Hypertension, infection, rupture, hemorrhage
- Excellent prognosis for vast majority of incidental, benign adrenal cysts
- Prognosis for pseudocysts secondary to adrenal neoplasm depends upon tumor histology
- ## Treatment
- No treatment required usually
- Imaging follow-up typically performed
- Intensity and length of surveillance not defined
- Cysts may enlarge over time
- Endocrine evaluation (cortisol, metanephrine, etc.) performed
- Surgical resection if symptomatic, underlying adrenal neoplasm
- Laparoscopic resection preferred
# DIAGNOSTIC CHECKLIST
- ## Consider
- Complicated cyst may suggest underlying adrenal neoplasm
- Clinical history, biochemical evaluation, and prior imaging helpful
- ## Image Interpretation Pearls
- Simple adrenal cyst: Scant septation, no enhancement, thin rim calcification
- Likely benign endothelial cyst or pseudocyst
- Coronal imaging helpful to determine organ of origin (and exclude exophytic renal or pancreatic cyst)
- Complicated cyst: High attenuation, thick enhancing wall, &/or septations
- Complexity may suggest underlying adrenal neoplasm and secondary pseudocyst
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