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[Eosinophilic cellulitis--clinical and histological aspects].

Eosinophilic cellulitis (Wells' syndrome) is a rare skin disease whose aetiology is still unknown. The onset is acute, and different disease stages may exist simultaneously during the course. Histological examination shows flame figures as a characteristic, but not pathognomonic, feature. In later stages the infiltrate adopts granulomatous characteristics. Malignant haematological disorders, which frequently occur with this disease, should be excluded.

Cellulitis↗

Prophylaxis for recurrent cellulitis complicating venous and lymphatic insufficiency.

Serious cellulitis, a common acute illness, frequently is associated with underlying venous and lymphatic compromise. The process is easily treated but, when recurrent, is associated with significant morbidity. Local measures, such as support hose and elimination of tinea pedis, have a role in its therapy but do not uniformly prevent recurrence. Prophylactic antibiotic therapy modeled after rheumatic fever prophylaxis can be effective in the prevention of this process.

Cellulitis↗

[Extensive cellulitis during chicken-pox. Six causes (author's transl)].

The authors report 6 cases of extensive cellulitis, in 6 children with chicken-pox. This is a rare complication during this disease. If streptococcal etiology is not always proved, clinical aspect and the dramatic reponse to treatment by penicillin G, characterize this kind of complication.

Cellulitis↗

An unusual case of orbital cellulitis.

Munchausen's syndrome, an unusual disorder related to malingering and hysteria, is occasionally seen by the ophthalmologist. Munchausen patients deliberately deceive and attempt to manipulate physicians 'through factitious signs and symptoms. They know they are acting, yet appear unable to control their actions. Unnecessary medical workups and inappropriate surgical interventions are common with this perplexing syndrome. An unusual case of orbital cellulitis that illustrates a number of these features is illustrated and the syndrome is reviewed.

Adult↗

[Eosinophilic cellulitis (Wells syndrome)].

There is a 37 years old patient with a erythemato-nodular pathology on her lower limbs, which has relapsed during three years. The characteristics of the eosinophilic cellulitis are observed in the microscopic study. The clinical and laboratory attributes of this entity are discussed, according to the world medical literature.

Adult↗

[Canyon-varices. Consequence and cause of sclerous cellulitis and their treatment].

Cutaneous and subcutaneous sclerosis of venous origin ("hypodermite chronique" to the French and "indurated cellulitis" to the Anglo-saxons) is always created by a "varicose vein-canyon", which communicates with one or several inadequate perforating? Varicose vein-canyons, or rather the circulatory and hypertensive disturbances that they engender, are without doubt mainly responsible for chronic panniculitis. It is extremely important to inactivate them to bring about regression of the sclerosis. The various ways of tackling the problem are based on three different principles: --contrasting the reflux from varicose vein-canyons by external compression; --cutting only vertical long reflux, by ablation or sclerosis of the inadequate saphenous veins and the other proximal varicose veins; --adding to the suppression of the long reflux by interruption of short reflux in the legs. The author insists yet again on the value of the "Glauco Bassi hook method", for which panniculitis is a choice indication, either because is enables the largest of the varicose vein-canyons (the "Leonardo vein") to be reached easily (and sometimes even to remove a few centimeters by rolling around forceps introduced into two incisions ten millimetres long at the most), or because there are few alternatives for interrupting the leakage points, if "sunk" varicose-veins are involved.

Cellulitis↗

Diplococcus pneumoniae. Cellulitis in drug addicts.

Cellulitis caused by Diplococcus pneumoniae was diagnosed in two heroin users. To our knowledge, this medical emergency, clinically indistinguishable from deep fasciitis of pyomyositis, has not previously been reported as having been caused by the agent identified in these two patients.

Adult↗

[Generalized morphea-like progressive systemic sclerosis with anticentromere antibodies and eosinophilic cellulitis].

A 67-year-old woman without any history of exposure to organic solvents suffered from Raynaud's phenomenon, sclerodactylia, contracture of finger joints, diffuse pigmentation, pulmonary fibrosis, and generalized morphea-like eruptions on the trunk; she was diagnosed as generalized morphea-like progressive systemic sclerosis. She had a high titer of anticentromere antibody in her serum without any symptoms of CREST syndrome. She also had eosinophilic cellulitis on her extremities, which subsided within 6 months, and seemed to be due to a hypersensitivity reaction to mosquito bites. The occurrence of these two diseases together in our case may suggest some similarities in their pathogenesis.

Aged↗

[Cellulitis, Haemophilus meningitis and measles. Apropos of a case report].

We report in a 13 months old child, with measles, a case of cellulitis, otitis and meningitis due to ampicillin-resistant Haemophilus influenzae Two facts are emphasized: the promoting aspect of measles/malnutrition and the empirical treatment of meningitis in resistant Haemophilus influenzae in tropical areas.

Anti-Bacterial Agents↗

[Orbital cellulitis after a dental infection].

Blindness as a complication of a dental infection is rare. A nineteen-year-old male is presented with an apical abscess, leading to a maxillary sinusitis, orbital cellulitis and an imminent cavernous sinus thrombosis.

Adult↗

Facial cellulitis responsive to flucloxacillin in acute leukemia.

A severely neutropenic patient, undergoing bone marrow transplantation for acute leukemia, experienced bilateral facial cellulitis accompanied by high fever and a facial folliculitis. All resolved with the addition of flucloxacillin to existing antibiotics suggesting a causal role for staphylococci.

Acute Disease↗

[Diffuse gangrenous cervicofacial cellulitis of stomatologic origin in 7 patients with HIV-1 infection].

A new clinical aspect of AIDS in Africa is represented by acute gangrenous cervico-facial cellulitis. In most of cases, the infection was due to infected tooth. Seven patients presenting with such clinical findings were HIV-1 infected (Western Blot). Bacteriological investigations failed to show bacteria responsible of these syndromes except for 4 cases. All patients healed after surgical treatment done in emergency and antibiotherapy. No mediastinal localisation was noticed. Prevention by removing all infected teeth must be emphasized in HIV infected patient.

Acquired Immunodeficiency Syndrome↗

The red eye. Infectious conjunctivitis, keratitis, endophthalmitis, and periocular cellulitis.

Patients presenting with a red eye may have a minor, self-limited inflammation of the ocular surface or a vision-threatening infection such as endophthalmitis or orbital cellulitis. Careful evaluation of distinctive clinical signs is necessary to determine the level of ocular involvement. A knowledge of the common microorganisms causing various eye infections (Table 6) can provide the basis to guide appropriate laboratory investigation and initial therapy. Detailed reference textbooks on ocular infection should be available, and ophthalmologic consultation should be considered in these cases to assist in diagnostic investigations and to monitor potential ocular complications.

Cellulitis↗

Hyperfibrinolysis in a patient with cellulitis.

A case of acute hyperfibrinolysis complication in cellulitis was reported. The bleeding did not stop for two days because of hematological defect. After giving antifibrinolysin and treating the etiologic factor, the bleeding stopped within a few hours. One should be aware that excessive bleeding in infection can possibly be caused by hyperfibrinolysis.

Acute Disease↗

Serious bacterial cellulitis of the periorbital area in two patients with systemic lupus erythematosus.

We describe the occurrence of bacterial cellulitis in the periorbital area of 2 patients with systemic lupus erythematosus (SLE). In both patients the antibacterial activity of polymorphonuclear leucocytes was normal. The opsonic capacity of serum was defective in one patient (corresponding to decreased levels of the 4th component of complement) and normal in the other. Seemingly minor bacterial infections of the skin in patients with SLE should warrant aggressive antimicrobial treatment.

Adolescent↗

Intramuscular injection techniques and the development of clostridial myositis or cellulitis in horses.

A survey of 584 veterinarians in equine practice was performed to determine their intramuscular injection techniques and the influence of those techniques on the development of clostridial myositis or cellulitis. Usable responses were obtained from 439 veterinarians (75.2%). Of these, 414 used a new needle and syringe for each injection, 241 swabbed the site with a cleansing/disinfectant agent, and 242 swabbed the top of multidose injection bottles with a similar solution. Only 2 clipped the hair at the injection site. Twenty eight of the respondents reported that at least 1 horse developed a clostridial infection at the injection site following 1 of their injections. None of the various injection techniques had a significant influence on the development of clostridial infection at the injection site.

Animals↗

[Orbital cellulitis following surgery of strabismus].

The authors report a case of orbital cellulitis after strabismus surgery. Diagnosis was confirmed by computerized tomography. Subsequent therapy and follow-up are discussed. Attention is drawn to the importance of this syndrome.

Cellulitis↗