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TLDR
A rare case of hidradenitis suppurativa (HS), diagnosed by definition criteria, with multiple subcutaneous abscesses with spontaneous drainage of pus, sub cutaneousindurations and scars in bilateral inguinal areas, which had appeared 10 years prior and rapidly increased in number.
Abstract
lated (to a maximum of 40 mg/day) or tapered according toUC activity. She was taking 5 mg/day at the initial visit to us.Physical examination showed multiple subcutaneousabscesses with spontaneous drainage of pus, subcutaneousindurations and scars in bilateral inguinal areas (Fig. 1a), butneither axillae nor buttocks were involved. Bacterial culturesyielded Streptococcus anginosus. Histological examinationshowed increase of collagenous fibers and infiltration of inflam-matory cells such as lymphocytes and neutrophils in the deepdermis (Fig. 1b), containing a number of CD3-, 4- and interleu-kin (IL)-17-positive cells (Fig. 1c). She was treated with oral anti-biotics (minocycline 200 mg/day). Additionally, she hadbrownish dermal nodules scattered on her trunk and legs(Fig. 1d), which had appeared 10 years prior and rapidlyincreased in number. Physical examination revealed seven nod-ules in total, but she denied familial occurrence. Histology ofthose nodules showed an ill-defined proliferation of fibrohistio-cytic cells in the dermis, containing foamy histiocytes (Fig. 1e).Toluidine blue stain revealed a number of mast cells in theperipheral layers of the fibrotic lesions (Fig. 1f), correspondingto the IL-17-positive cells on serially cut sections (Fig. 1g).We herein described a rare case of hidradenitis suppurativa(HS), diagnosed by definition criteria,

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Sweet's syndrome revisited: a review of disease concepts

TL;DR: The evolving and new concepts of this dermatosis that are discussed include: Sweet's syndrome occurring in the clinical setting of a disease‐related malignancy, or medication, or both; detection of additional sites of extracutaneous Sweet's syndrome manifestations; discovery of additional Sweet'S syndrome‐associated diseases; variability of the composition and/or location of the cutaneous inflammatory infiltrate in Sweet' s syndrome lesions; and additional efficacious treatments for Sweet’s syndrome.
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Neutrophilic panniculitis associated with myelodysplastic syndromes

TL;DR: Four-mitTon parallin-embedded sections were stained with an indirect immunolluorescent method using affinity-puriHed rahhii anti-.MllP o\'erlaid wilh lluorescein Isothiocyanale conjugated goat antirabhit IgCI to assess cellular staining and extracellular protein deposition.
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Neutrophilic panniculitis with myelodysplastic syndromes presenting as pustulosis: case report and review of the literature.

TL;DR: A 59‐year‐old patient who initially was diagnosed with myelodysplastic syndrome and developed a sudden onset of widespread pustulosis and erythematous indurated papules is reported to have disappeared completely after treatment with systemic corticosteroids.