Abstract |
We report here a very rare case of MCTD complicating double cancer. A 43-year-old woman with suspected MCTD was admitted because of high fever and lymphadenopathy. The laboratory findings indicated high titers of speckled ANA, anti-RNP, DNA and Scl-70, but anti-Sm. SS-A and SS-B was not detected. Chest CT and Spirogram revealed lung fibrosis, restrictive ventilatory impairment, and decreased diffusion capacity. Biopsy specimen by gastric fiberscope s screening indicated II c advanced type of poorly differentiated adenocarcinoma. After subtotal gastrectomy, she had high fever, pleuritis, leukopenia, butterfly erythema and hypoxemia, which were improved by 30 mg/day of oral prednisolone. One year after from the last operation, she had contact bleeding, and squamous cell carcinoma of the uterine cervix was diagnosed. She had Raynaud's phenomenon 6 months after from hysterectomy.
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Authors | M Katayama, I Tanaka, Y Hosako, N Hama, T Yamada, S Inada, M Goto |
Journal | Ryumachi. [Rheumatism]
(Ryumachi)
Vol. 35
Issue 1
Pg. 85-9
(Feb 1995)
ISSN: 0300-9157 [Print] Japan |
PMID | 7732496
(Publication Type: Case Reports, English Abstract, Journal Article, Review)
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Topics |
- Adenocarcinoma
(complications)
- Adult
- Carcinoma, Squamous Cell
(complications)
- Female
- Humans
- Mixed Connective Tissue Disease
(complications)
- Neoplasms, Multiple Primary
- Stomach Neoplasms
(complications)
- Uterine Cervical Neoplasms
(complications)
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