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hidradenitis/demam
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Association of hidradenitis suppurativa and familial Mediterranean fever: A case series of 6 patients.
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OBJECTIVE
Familial mediterranean fever (FMF) is the most common monogenic autoinflammatory disease. Hidradenitis suppurativa (HS) is an inflammatory cutaneous disease. Those diseases can occur simultaneously among the same individual. Our objective was to describe the features of patients displaying
Familial Mediterranean fever patients with hidradenitis suppurativa.
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BACKGROUND
Hidradenitis suppurativa (HS) has recently been described as a component of two autoinflammatory syndromes: PASH (pyoderma gangrenosum, acne, and HS) and PAPASH (pyoderma gangrenosum, acne, pyogenic arthritis, and HS). These associations together with others such as inflammatory bowel
Hidradenitis suppurativa and Mediterranean fever gene mutations.
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Reply to: "Hidradenitis suppurativa and Mediterranean fever gene mutations".
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Hidradenitis Suppurativa Is Associated with Familial Mediterranean Fever-A Population-Based Study.
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[Adult idiopathic neutrophilic eccrine hidradenitis treated with colchicine].
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BACKGROUND
Neutrophilic eccrine hidradenitis (NEH) is a rare disease belonging to the group of neutrophilic dermatoses. It has a characteristic histopathologic pattern, with necrosis of the eccrine glands and a local neutrophilic infiltrate. It occurs mostly in patients receiving chemotherapy for
Hidradenitis suppurativa and vasculitis: A case series and literature review of a rare association.
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Hidradenitis suppurativa is a chronic inflammatory skin disease with dysregulation of the immune system. Its pathophysiology is not clear, and it has been reported in association with various inflammatory disorders such as pyoderma gangrenosum, arthritis, familial Mediterranean fever and
Recurrent palmoplantar hidradenitis in children.
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BACKGROUND
There are several reports of tender, erythematous plantar nodules occurring in pediatric patients. Despite similar morphological features, the histologic findings in these lesions have been quite diverse. A new entity called idiopathic plantar hidradenitis (also termed neutrophilic
[Pseudomonas eccrine hidradenitis in a child revealing acute lymphoblastic leukemia].
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BACKGROUND
We report the case of a Pseudomonas (P.) aeruginosa eccrine hidradenitis in a child, or a "Pseudomonas Hot Foot Syndrome", revealing an acute lymphoblastic leukemia.
METHODS
A 10 year-old girl consulted for the sudden onset of painful and necrotic palmoplantar nodules in a context of
[Plantar hidradenitis].
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Tender, plantar nodules occurring in pediatric patients can be associated to different clinical entities, despite similar morphological features, therefore dermatopathology is the best technique for the definitive diagnosis. We describe the case for a 12-year-old patient with tender, red nodules on
A preliminary report on the use of Staphage Lysate for treatment of hidradenitis suppurativa.
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Eight patients, 7 with hidradenitis suppurativa and 1 with chronic recurrent staphylococcal abscess, all of whom failed to respond to antibiotic therapy, conservative therapeutic measures, and surgery, were experimentally placed on Staphage Lysate. Treatment after appropriate skin testing consisted
Neutrophilic eccrine hidradenitis in two patients treated with BRAF inhibitors: a new cutaneous adverse event.
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Neutrophilic eccrine hidradenitis (NEH) is a rare neutrophilic dermatosis, first described in patients undergoing chemotherapy for a malignant haemopathy. It has polymorphous clinical features and the association of both clinical and histological features is necessary to make a diagnosis. We report
Neutrophilic eccrine hidradenitis simulating orbital cellulitis.
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Orbital swelling in patients with cancer can reflect neoplastic or infectious processes. Accurate diagnosis can be especially difficult in the face of associated fever and neutropenia. We treated a 30-year-old man undergoing induction chemotherapy for acute myelogenous leukemia, who had fever of
Neutrophilic eccrine hidradenitis associated with Hodgkin's disease and chemotherapy. A case report.
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A 44-year-old man with Hodgkin's disease developed fever and erythematous macules and plaques associated with doxorubicin, bleomycin, vinblastine, and dacarbazine chemotherapy. Biopsy results demonstrated a neutrophilic infiltrate around sweat glands and degeneration of eccrine glands. These
Cutaneous histopathology of Rocky Mountain spotted fever.
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The dermatologic diagnosis of Rocky Mountain spotted fever (RMSF) is often presumptive; the clinical presentation includes skin rash and febrile illness with or without a clear history of tick bite. The characteristic cutaneous manifestations include a generalized skin eruption with purpuric,
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