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Biomedical subjects

J M Mascaro

Publications and source records attributed to J M Mascaro.

At least 109 records · Page 6Linked to original sources
PubMed1980

Acute and chronic graft-vs-host reaction in skin: report of two cases.

The cutaneous changes of the acute form of graft-vs-host reaction are described in two patients who underwent bone marrow transplantation for treatment of severe aplastic anaemia. One patient went on to develop a chronic reaction of the lichenoid type. Histopathology confirmed the presence of 'satellite cell necrosis' from the acute stage of the disease onwards. Direct immunofluorescence showed deposits of immunoglobulin (IgG, IgM), fibrinogen and complement on the necrotic keratinocytes, whilst the basement membrane was positive for C3. These findings suggest that humoral immunity as well as cellular immunity may play a part in the production of the rash.

Acute Disease↗
PubMed1980

[Pili canaliculi (uncombable hair syndrome or spun glass hair syndrome). A scanning electron microscope study of ten new cases (author's transl)].

"Uncombable hair" is the denomination applied to a new abnormality of the hair, being characterized by its arranged in bundles disposed in different directions and which are irreductible on combing. It may have a familial trait and starts at the age of 3 months onwards. It appears in children of both sexes, whose hair becomes dry, tightly curled, shiny, lighter and impossible to comb. There are no accompanying abnormalities in the development. Neither have any biological changes been registered. The clinical and ultrastructural aspects of 10 cases of children affected with "uncombable hair" are presented. At the scanning electron microscope we have observed longitudinally disposed canalicular formations on the cuticular surface of 50 p. 100 of hair taken from each patient. The canal is, in some zones, more excavated than in others, occasionaly has an irregular outline and sometimes is uniformly located nearly along the whole length of the hair. The transversal section shows triangular aspects, kidney-shaped or completely irregular. We agree with Dupré to use the term pili canaliculi for the defect shown by these patients.

Adolescent↗
PubMed1977

Scanning electron microscopic and X ray microanalysis study of the mineral deposits in pseudoxanthoma elasticum.

A skin biopsy of a 37 year old man with typical lesions of pseudoxanthoma elasticum (P.E.) associated with angioid streaks (Groenbald-Strandberg Syndrom) was examined with a scanning E.M. (SEM) and a SEM provided with a X ray micro-analyser. The SEM provided with X ray microanalyser enabled us to see the correspondence between the crystalline deposits and a calcium salt. The potassium, sodium and magnesium analysis of the specimen permits us to verify that the P.E. dermis is rich in K and poor in Mg.

Adult↗
PubMed1977

[Contact dermatitis caused by ethylene oxide].

A case of contract sensitization to the ethylene oxide by a mask sterilized with this substance is reported. The mask was correctly sterilized but the ethylene oxide was not completely evaporised. The path tests were positive in the patient but negative in 25 control subjects. The patch tests with the international series and with all the elements of the mask were negative. The possible troubles of ethylene oxide and the sterylisation methodes of this substance are reviewed.

Dermatitis, Contact↗
PubMed1977

[Gunther's congenital erythropoietic porphyria in an 8-month old girl (author's transl)].

A typical case of congenital erythropoietic porphyria in a 8 month old girl is reported (photosensitive blistering syndrome, hypertrichosis; erythrodontia; fluorescence of urine, teeth, erythrocytes and myeloblasts; splenomegaly; anaemia). Porphyrins, isomers I, were present in urine and blood. In faeces a porphyrin-X-like substance migrating as PX was detected; this porphyrin was finally identified as CP I unusually difficult to extract because of the presence of a banding and fluorescence quenching agent probably of exogenous origin. The usual methods are not always able to extract and to identify the faecal porphyrins.

Bone Marrow Diseases↗