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Primary Adrenal Cortical Carcinoma

Primary Adrenal Cortical Carcinoma

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Incidental Finding on r/o PE Study

Incidental Finding on r/o PE Study

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Adrenal Carcinoma in Patient with Ulcerative Colitis

Adrenal Carcinoma in Patient with Ulcerative Colitis

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Primary Adrenal Carcinoma with Positive Nodes. Presented with Cushings Syndrome

Primary Adrenal Carcinoma with Positive Nodes. Presented with Cushings Syndrome

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Primary Adrenal Carcinoma: Presentation

  • Hormonal abnormality (i.e. Cushings)(40-60%)
  • Flank or back pain (30%)
  • Incidental finding on CT (10-15%)

 

“The most common clinical presentation for functioning ACC is Cushing’s syndrome, characterized by symptoms related to excess corticosteroid synthesis including truncal obesity, diabetes, hypertension, easy bruising, and menstrual cycle irregularities. In females, virilization resulting from excess androgens may accompany signs of excess cortisol. A small percentage of male patients, present with signs of estrogen excess, such as gynecomastia, breast tenderness, decreased libido, and testicular atrophy.”
Adrenal cortical carcinoma: pathology, genomics, prognosis, imaging features, and mimics with impact on management
Ayahallah A. Ahmed et al.
Abdom Radiol 2020 Apr;45(4):945-963

 

“Although the majority of ACCs develop sporadically, many cases arise in association with various familial cancer syndromes including Li–Fraumeni, Beckwith–Wiedemann, and Lynch syndromes. Several genetic alterations have been noted to play an important role in the pathogenesis of ACC. Most of the drivers for the pathogenesis of ACC are related to mutations or downregulation of tumor suppressor genes, overexpression of certain growth factors, chromosomal aberrations, and dysregulation of certain important signaling pathways.”
Adrenal cortical carcinoma: pathology, genomics, prognosis, imaging features, and mimics with impact on management
Ayahallah A. Ahmed et al.
Abdom Radiol 2020 Apr;45(4):945-963

 

“ACCs are typically large, with roughly 70% of tumors larger than 6 cm at the time of diagnosis. Size of the adrenal tumor, pattern of contrast enhancement, and degree of heterogeneity by CT are all important predictors of the malignant potential of the adrenal lesion. ACC is typically heterogeneous by CT and displays mixed intratumoral attenuation. An attenuation value of more than 10 HU on non-contrast CT has high sensitivity for detecting malignancy (93%), but a specificity of only 71–73%. Contrast enhancement is heterogeneous and may be increased peripherally due to central necrosis.”
Adrenal cortical carcinoma: pathology, genomics, prognosis, imaging features, and mimics with impact on management
Ayahallah A. Ahmed et al.
Abdom Radiol 2020 Apr;45(4):945-963

 

“Although the presence of macroscopic fat is most commonly seen in benign myelolipoma, ACC may show areas of macroscopic fat as well. Other imaging and biochemical features should be kept in consideration to differentiate this rare manifestation of ACC from myelolipoma, as previously discussed. With any adrenal lesion, the appropriate workup depends on a variety of factors. Incorporating clinical, imaging, and biochemical data allow the formulation of a proposed systematic approach.”
Adrenal cortical carcinoma: pathology, genomics, prognosis, imaging features, and mimics with impact on management
Ayahallah A. Ahmed et al.
Abdom Radiol 2020 Apr;45(4):945-963

 

Primary Adrenal Lymphoma: CT Appearance

  • It is characterized by large tumors, exceeding 10 cm in diameter, with a growth pattern of infiltration.
  • Masses generally expand and infiltrate the glands, maintaining their triangular appearances.
  • some primary adrenal lymphomas may manifest as masses with necrotic or cystic components and heterogeneous, moderate enhancement , as occurred in one of our cases making it impossible to differentiate from primary adrenal cortical carcinoma, pheochromocytomas, or metastatic disease.

 

Follicular Lymphoma

Follicular Lymphoma

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Back Pain

Back Pain

 

Primary Lymphoma of the Adrenal Gland

Primary Lymphoma of the Adrenal Gland

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Abdominal Pain and FUO

Abdominal Pain and FUO

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

Large Adrenal Masses

 

 
 

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