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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---
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title: "Adrenal Cyst"
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docid: "c5d717a3-3d6e-4e86-9efe-1ad0ec14740f"
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breadcrumbs:
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- "Genitourinary"
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- "Diagnosis"
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- "Adrenal"
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- "Benign Neoplasms"
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- "Adrenal Cyst"
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---
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# KEY FACTS
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- ## Imaging
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- "Adrenal cyst" is descriptive term, not pathological diagnosis
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- True adrenal cysts
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- Majority are endothelial cysts (lymphangiomas)
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- Epithelial cysts exceedingly rare
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- Simple, or minimally complex, adrenal cyst, thin rim calcification, no enhancement
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- Pseudocysts
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- Prior hemorrhage inferred
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- Nonenhancing but complex contents and wall calcification
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- Relevant history (extraadrenal malignancy, rapid growth), biochemical evaluation (cortisol, metanephrines): Consider underlying adrenal neoplasm
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- Enhancing soft tissue components may suggest adrenal mass hemorrhage and pseudocyst formation
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- Parasitic (echinococcal) cyst
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- Rare outside endemic areas
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- Typically in setting of generalized echinococcus
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- ## Top Differential Diagnoses
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- Adrenal adenoma
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- CECT: Enhancing mass without visible wall or peripheral calcifications
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- Gastric diverticulum
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- Air-, fluid-, or contrast-filled mass with no enhancement of contents
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- Adrenal myelolipoma
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- Macroscopic fat
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- Necrotic adrenal tumor
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- Complex wall with heterogeneous contents
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- Retroperitoneal bronchogenic cyst
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- ## Clinical Issues
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- No treatment required usually
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- Imaging surveillance performed, although intensity and length of follow-up not defined
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- Biochemical evaluation (cortisol, metanephrines) routinely performed to exclude underlying adrenal neoplasm
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- Surgical resection for complex cyst with enhancing components, or symptomatic cyst
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- ## Diagnostic Checklist
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- Complicated cyst has high attenuation, thick enhancing wall, &/or septations
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# TERMINOLOGY
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- ## Definitions
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- "Adrenal cyst" is descriptive term, not pathological diagnosis
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- Can mean true cyst, pseudocyst, or cystic mass
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# IMAGING
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- ## General Features
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- ### Best diagnostic clue
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- Well-defined, nonenhancing, water-density adrenal mass ± calcifications
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- ### Location
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- Suprarenal
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- Unilateral > bilateral (8-10% of cases)
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- ### Size
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- < 5 cm (50%), up to 20 cm
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- ## CT Findings
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- ### NECT
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- Unilocular or multilocular mass
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- Well-defined, round to oval, homogeneous mass usually with water (0 HU) or near-water density
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- Higher- or mixed-attenuation mass (hemorrhage, intracystic debris, crystals)
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- Wall usually very thin
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- ↑ wall thickness, up to 3 mm for complex cysts
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- Calcifications
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- Rim-like or nodular (51-69%)
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- Centrally in intracystic septation (19%)
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- Punctate within intracystic hemorrhage (5%)
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- ### CECT
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- No central enhancement ± wall enhancement
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- Coronal reformats helpful to determine organ of origin if large cyst
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- ## MR Findings
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- ### T1WI
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- Homogeneous, hypointense mass
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- Hyperintense mass (hemorrhage)
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- ### T2WI
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- Hyperintense mass
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- ## Ultrasonographic Findings
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- Simple or septated suprarenal cyst
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- Shadowing from calcification
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- Real-time examination helpful to differentiate adrenal cyst from adjacent (renal, pancreatic) cyst
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- ## Imaging Recommendations
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- ### Best imaging tool
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- CECT or MR; US for confirmation
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# DIFFERENTIAL DIAGNOSIS
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- [Adrenal Adenoma](/document/adrenal-adenoma/e2916d86-5f9f-4dd3-9576-1a7b89d8dda0)
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- NECT: Lipid-rich adenoma (< 10 HU) mimics adrenal cyst
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- Peripheral or septal calcification favors adrenal cyst
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- CECT: **Enhancing mass** without visible wall or peripheral calcifications
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- Assess washout kinetics to diagnose lipid-poor adenoma
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- MR: Signal suppression at out-of-phase, chemical-shift imaging
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- US: Solid adrenal lesion
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- [Gastric Diverticulum](/document/gastric-diverticulum/eeb101f0-8bdf-4771-b44a-fe6e73b3a463)
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- May simulate left adrenal cyst
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- Air-, fluid-, or contrast-filled suprarenal mass
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- No enhancement
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- Normal adjacent adrenal gland
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- [Adrenal Myelolipoma](/document/adrenal-myelolipoma/5813a554-06a4-4696-af71-7ce50693039d)
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- Fat (not fluid) attenuation mass
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- ## Necrotic Adrenal Tumor
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- Primary (pheochromocytoma or carcinoma) or metastatic
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- Clinical history, biochemical evaluation, lesion complexity suggest correct diagnosis
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- Enhancing soft tissue components
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- ## Retroperitoneal Bronchogenic Cyst
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- Rare, benign, suprarenal fluid or soft tissue attenuation lesion
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- Adjacent to but separate from adrenal gland
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- ## Renal Cyst
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- Coronal MR/CT or US useful to determine organ of origin of large, retroperitoneal cystic lesions
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# PATHOLOGY
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- ## General Features
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- ### Etiology
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- Congenital (endothelial, epithelial) cysts
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- Acquired (post hemorrhagic, inflammatory) pseudocysts
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- Cystic, hemorrhagic degeneration of underlying adrenal neoplasm
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- ## Staging, Grading, & Classification
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- Accepted classification scheme
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- Pseudocyst
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- Most common type of cystic adrenal lesion in surgical series
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- No epithelial or endothelial lining: Fibrous cyst wall
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- Potentially as complication of prior trauma or hemorrhage though history of such often not elicited
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- May be associated with underlying adrenal neoplasm (pheochromocytoma, adrenal carcinoma, myelolipoma)
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- Attenuation and complexity at imaging varies depending upon hemorrhagic component
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- Wall and septal calcification common
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- Endothelial cyst
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- Subtypes: Lymphangiomatous and hemangiomatous
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- True cyst: Endothelial lining
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- Originate from preexisting vascular malformation or obstructed, ectatic lymphatic channels
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- Thin rim calcification typical
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- Epithelial cyst
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- Extremely rare: No acinar structures within normal adrenal gland
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- Mesothelial origin suggested (mesothelial cells potentially incorporated within adrenal gland during embryogenesis)
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- Parasitic (hydatid) cyst
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# CLINICAL ISSUES
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- ## Presentation
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- ### Most common signs/symptoms
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- Typically asymptomatic
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- Larger cysts may be symptomatic
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- Abdominal pain
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- Hemorrhage
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- Clinical history (malignancy, hypertension) elicited
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- May indicate cystic degeneration of underlying adrenal neoplasm (e.g., metastasis, pheochromocytoma)
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- Diagnosis
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- Usually incidental finding at imaging
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- Endocrine-biochemical evaluation performed to exclude underlying functional adrenal tumor
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- ## Demographics
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- ### Age
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- Any, though patients 20-50 years of age most common
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- ### Sex
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- M:F = 1:3
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- ### Epidemiology
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- Uncommon entity: Autopsy incidence 0.064-0.18%
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- Accounts for 1% of incidental adrenal lesions in large imaging series
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- ## Natural History & Prognosis
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- Complications
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- Hypertension, infection, rupture, hemorrhage
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- Excellent prognosis for vast majority of incidental, benign adrenal cysts
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- Prognosis for pseudocysts secondary to adrenal neoplasm depends upon tumor histology
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- ## Treatment
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- No treatment required usually
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- Imaging follow-up typically performed
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- Intensity and length of surveillance not defined
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- Cysts may enlarge over time
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- Endocrine evaluation (cortisol, metanephrine, etc.) performed
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- Surgical resection if symptomatic, underlying adrenal neoplasm
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- Laparoscopic resection preferred
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# DIAGNOSTIC CHECKLIST
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- ## Consider
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- Complicated cyst may suggest underlying adrenal neoplasm
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- Clinical history, biochemical evaluation, and prior imaging helpful
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- ## Image Interpretation Pearls
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- Simple adrenal cyst: Scant septation, no enhancement, thin rim calcification
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- Likely benign endothelial cyst or pseudocyst
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- Coronal imaging helpful to determine organ of origin (and exclude exophytic renal or pancreatic cyst)
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- Complicated cyst: High attenuation, thick enhancing wall, &/or septations
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- Complexity may suggest underlying adrenal neoplasm and secondary pseudocyst
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35fa0290-3451-422f-8726-c69b68aadbb5
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