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CASE 11
• 45year male
• Presented with left flank pain
• USG: 9X10 cm mass lesion was noted in the
left lumbar retroperitoneal region.
• FNAC- under guidance
• Other investigations: RFT, LFT, routine
biochemical investigations
• Complete hemogram
• USG : retroperitoneal sarcoma
• CT: Liposarcoma
Response
• Soft tissue tumour
• Malignant vascular tumour
• Paraganglioma
MYELOLIPOMA
ADRENAL MYELOLIPOMA
Adrenal myelolipoma is a benign tumour.
In 1905 Gierke first described the occurrence
of a mass lesion in the adrenal glands.
They were subsequently termed formations
myelolipomatoses by Oberling in 1929.
Myelolipomas account for approximately 3 to 5% of all
primary adrenal tumors.
Thought to arise from metaplasia of undifferentiated
stromal cells.
5th to 7th decades of life
Usually solitary
Associations :
 with overproduction of dehydroepiandrosterone-
sulphate (DHEAS),
 congenital adrenal hyperplasia caused by 21-
hydroxylase deficiency,
 congenital adrenal 17 α-hydroxylase deficiency,
 Cushing disease,
 Conn syndrome,
 adrenal insufficiency, and pheochromocytoma.
• Gross: capsulated, lobulated, yellow to red
brown depending upon the relative
proportion of fat and myeloid cells.
• Microscopy: islands of fat cells intermixed
with hematopoietic stem ells, mainly myeloid
and erythroid precursors, along with
scattered megakaryocytes.
• SURGICAL EXCISION
Case 11
Case 11

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Case 11

  • 1.
  • 3. • 45year male • Presented with left flank pain • USG: 9X10 cm mass lesion was noted in the left lumbar retroperitoneal region. • FNAC- under guidance
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10. • Other investigations: RFT, LFT, routine biochemical investigations • Complete hemogram • USG : retroperitoneal sarcoma • CT: Liposarcoma
  • 11.
  • 12.
  • 13.
  • 14. Response • Soft tissue tumour • Malignant vascular tumour • Paraganglioma
  • 15.
  • 17. ADRENAL MYELOLIPOMA Adrenal myelolipoma is a benign tumour. In 1905 Gierke first described the occurrence of a mass lesion in the adrenal glands. They were subsequently termed formations myelolipomatoses by Oberling in 1929.
  • 18. Myelolipomas account for approximately 3 to 5% of all primary adrenal tumors. Thought to arise from metaplasia of undifferentiated stromal cells. 5th to 7th decades of life Usually solitary
  • 19. Associations :  with overproduction of dehydroepiandrosterone- sulphate (DHEAS),  congenital adrenal hyperplasia caused by 21- hydroxylase deficiency,  congenital adrenal 17 α-hydroxylase deficiency,  Cushing disease,  Conn syndrome,  adrenal insufficiency, and pheochromocytoma.
  • 20. • Gross: capsulated, lobulated, yellow to red brown depending upon the relative proportion of fat and myeloid cells. • Microscopy: islands of fat cells intermixed with hematopoietic stem ells, mainly myeloid and erythroid precursors, along with scattered megakaryocytes. • SURGICAL EXCISION

Editor's Notes

  1. development and differentiation of either ectopic adrenal rests or hematopoietic stem cell rests in response to a triggering stimulus, particularly endocrine dysfunction. Other researchers found clonal cytogenetic abnormalities, which suggested it was of tumor origin [7]. Chromosomal translocations (3;21) (q25;p11) detected in myelolipomas and in benign lipomatous neoplasia seen in patients with acute myelogenous leukemia or myelodysplastic syndrome suggest the origin of this tumor to be bone marrow,