Mucinous cystadenocarcinoma

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Mucinous cystadenocarcinoma
Mucinous cystic tumor, atypical, uncertain malignant potential Case 252 (8211727496).jpg
Atypical goblet cells with focal tufting. The classification of these rare neoplasms is difficult and controversial. There appears to be a spectrum of mucinous cystic tumors ranging from those that are obviously benign (benign epithelium and no tumor invasion into surrounding lung) to those that exhibit invasion into surrounding lung tissue and are, therefore, malignant. In between is a group of neoplasms that exhibit epithelial atypia but no tumor invasion into lung tissue and the malignant potential of these is uncertain. This case appears to fall into that category. Focal cyst rupture with extravasation of mucin into surrounding lung tissue may occur with all types of mucinous cystic tumors.

Mucinous cystadenocarcinoma is a type of tumor in the cystadenocarcinoma grouping.

It can occur in the breast[1] as well as in the ovary.[2] Tumors are normally multilocular with various smooth, thin walled cysts. Within the cysts is found a haemorrhagic or cellular debris.[2]

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References

  1. Honma N, Sakamoto G, Ikenaga M, Kuroiwa K, Younes M, Takubo K (August 2003). "Mucinous cystadenocarcinoma of the breast: a case report and review of the literature". Arch. Pathol. Lab. Med. 127 (8): 1031–3. doi:10.5858/2003-127-1031-MCOTBA. PMID 12873181. Archived from the original on 2023-01-13. Retrieved 2022-04-25.
  2. 2.0 2.1 "Ovarian mucinous cystadenocarcinoma | Radiology Reference Article". Radiopaedia.org. Archived from the original on 25 April 2022. Retrieved 25 April 2022.
Classification