1980
DOI: 10.1016/s0190-9622(80)80229-5
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Secondary syphilis mimicking mycosis fungoides

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Cited by 10 publications
(7 citation statements)
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“… 6 Moreover, several other cases since Abell’s have made equally compelling histological arguments for a diagnosis of MF. 7 – 10 However, when reported, the T-cell receptor (TCR) gamma/beta gene rearrangement assay was negative, and in some of the cases the Warthin-Starry stain demonstrated spirochetes. 8 , 9 In our patient, MF was not a consideration based on the rapidity of the eruption and more aggressive pathology seen from the skin biopsies.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“… 6 Moreover, several other cases since Abell’s have made equally compelling histological arguments for a diagnosis of MF. 7 – 10 However, when reported, the T-cell receptor (TCR) gamma/beta gene rearrangement assay was negative, and in some of the cases the Warthin-Starry stain demonstrated spirochetes. 8 , 9 In our patient, MF was not a consideration based on the rapidity of the eruption and more aggressive pathology seen from the skin biopsies.…”
Section: Discussionmentioning
confidence: 99%
“…In 1980, Levin et al described a patient with compelling evidence for the diagnosis of MF, only to later be revealed as a strange case of secondary syphilis. 7 Since Levin’s report, there have been other documented cases of secondary syphilis mimicking MF. 8 – 10 Our patient highlights similar points, and, in addition, offers an etiology to the cause of rupioid syphilis in HIV underlining the importance of a detailed medical history and adequate laboratory tests in an HIV infected patient.…”
Section: Introductionmentioning
confidence: 99%
“…Hair loss can also occur (moth-eaten alopecia/alopecia syphilitica), typically affecting the scalp, but also the eyebrows or total body hair loss. Secondary syphilis has been termed the “great masquerader”, because its skin lesions show such diverse clinical and/or histologic morphologies, mimicking alopecia areata (130), bullous pemphigoid (131), cutaneous lymphoid hyperplasia (pseudolymphoma) (132–135), erythema multiforme (126, 136), granuloma annulare (43, 128, 137, 138), histiocytoma (34), leprosy (128, 139, 140), lichen planus (34, 126, 135, 141, 142), lupus erythematosus (43, 128, 143), mycosis fungoides (126, 144146), pemphigus vulgaris (147), pityriasis lichenoides et varioliformis acuta (PLEVA) (34, 126, 135), pruritic (eczematous) dermatoses (126, 128, 148), psoriasis (34, 128, 149, 150), pustular psoriasis (34, 128), sarcoidosis (34, 135, 151–155), small vessel vasculitis (156), suppurative folliculitis (157), superficial thrombophlebitis (158), Sweet’s syndrome (128, 159), tinea imbricata and erythema annulare centrifugum (34, 160), and urticaria (104). Ulcerative nodular presentations are rare and can occur secondary to follicular pustules (157, 161), or an obliterative endarteritis, known as lues maligna (162, 163).…”
Section: The Pathology Of Human Syphilismentioning
confidence: 99%
“…An unusual presentation in conjunction with failure to recognize the causes of rare false‐negative testing for secondary syphilis led to a delayed diagnosis in this patient. Although syphilis and mycosis fungoides have previously been reported to mimic one another both clinically and histopathologically, the potential for secondary syphilis to be misdiagnosed in this fashion is not generally appreciated 13–15. Recognition of the possibility of secondary syphilis occurred just in time to spare this patient the “rash decision” of treating him with cytotoxic therapy directed against CTCL.…”
Section: Commentarymentioning
confidence: 96%