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  Vol. 114 No. 8, August 1978 TABLE OF CONTENTS
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Granulomatosis Disciformis Chronica et Progressiva With Lymphadenopathy

Takashi Miura, MD; Yoshio Tanahashi, MD

Arch Dermatol. 1978;114(8):1224-1225.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

We report a case of granulomatosis disciformis chronica et progressiva (GDCP) in which the condition developed not only on the skin but also in the lymph node tissue.

REPORT OF A CASE

A 31-year-old man was admitted to our hospital with multiple skin lesions of about three months' duration. Examination showed multiple round or oval erythematous plaques that were distributed on the head, mandibular, pubic, and axillary regions, chest, back, and antecubital fossae. The borders of these plaques were firm, yellowish-reddish, sharply demarcated, and elevated from the skin surface like an embankment. The central parts were atrophic and depressed, and telangiectases and irregularly shaped white scars were noted (Fig 1). Secondary alopecia was observed on the head and axillary and pubic regions, and several ulcers were noted on the plaques. Several axillary and inguinal lymph nodes were palpable in fingertip sizes; they were relatively firm, but not adherent to the . . . [Full Text PDF of this Article]


Author Affiliations

From the Department of Dermatology, Tohoku University School of Medicine, Sendai, Japan.


Footnotes

Reprint requests to Department of Dermatology, Tohoku University School of Medicine, Sendai 980, Japan (Dr Miura).



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