Mixed connective tissue disease

Mixed connective tissue disease (MCTD) is a rare connective tissue disorder combining clinical features of systemic lupus erythematosus (SLE), systemic sclerosis (SSc), polymyositis (PM) (see these terms) and/or rheumatoid arthritis (RA).

Carcinoma

A malignant tumor arising from epithelial cells. Carcinomas that arise from glandular epithelium are called adenocarcinomas, those that arise from squamous epithelium are called squamous cell carcinomas, and those that arise from transitional epithelium are called transitional cell carcinomas (NCI Thesaurus).

Total: 4

(per page)

PMID (PMCID)
17409667	FEMALE
	[A case of hepatocellar carcinoma associated with mixed connective tissue disease].
	Monoe K, Kanno Y, Saito H, Abe K, Takahashi A, Takiguchi J, Rai T, Hikichi T, Ohira H. Nihon Shokakibyo Gakkai Zasshi. 2007;104(4):568-72.
	[A case of hepatocellar carcinoma associated with mixed connective tissue disease].
9133950	FEMALE	Child
	Anti-RNP antibody in a child with undifferentiated carcinoma and no evidence of mixed connective tissue disease.
	Foster HE, Malleson PN, Petty RE, Cabral DA. Br J Rheumatol. 1997;36(2):289-91.
	Anti-RNP antibody in a child with undifferentiated carcinoma and no evidence of mixed connective tissue disease.
9133950	FEMALE	Child
	Anti-RNP antibody in a child with undifferentiated carcinoma and no evidence of mixed connective tissue disease.
	Foster HE, Malleson PN, Petty RE, Cabral DA. Br J Rheumatol. 1997;36(2):289-91.
	She was initially suspected of having mixed connective tissue disease, but ultimately was found to have metastatic undifferentiated carcinoma with an unknown primary site.
2056737	MIXED_SAMPLE	Middle Aged
	[Postoperative infections in systemic immunocompromising diseases. A study of 6 patients].
	Bialasiewicz AA, Wilk CM, Ruprecht KW. Klin Monbl Augenheilkd. 1991;198(3):190-4.
	Six patients with postoperative endophthalmitis after elective intraocular surgery suffering from Sharp-syndrome, metastasizing antrum carcinoma, granulomatous vasculitis and immunosuppressive therapy, agranulocytosis, silico-tuberculosis and chronic lymphatic leukemia revealed traditionally pathogenic agents (Proteus mirabilis, P. aeruginosa, enterococci, coagulase-negative Staph).