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Biomedical subjects

J G Casas

Publications and source records attributed to J G Casas.

At least 19 recordsLinked to original sources

[Reproducibility of nuclear grade in breast neoplasm. A multicenter experience].

Nuclear grade is considered a valuable prognostic factor in mammary carcinomas. Since the histological diagnosis of most of these tumors is made by "non expert" pathologists, it was considered interesting to find out the reproducibility of general pathologists to define the nuclear grade. In order to do this, a series of 15 mammary carcinomas, 10 of them randomly selected and 5 because they were considered difficult to classify for nuclear grade, were examined separately by 10 general pathologists. In a first round of observation, each one of them graded the cases according to their own criteria as used routinely, and for a second round they followed a written guide. An analysis of variance was applied to the data and no significant differences were found between observers, neither in the randomly selected cases nor in the total series. The written guide, surprisingly, instead of lowering the differences, increased them. Analysis of the individual performance of observers showed two of them having a great variation between both rounds of observation, and this was considered to influence the results of the whole group. Interobserver performance to discriminate high grade tumors (G3) from the rest, showed a good correlation in all the participants. These results allow us to conclude that in this series, examined by general pathologists, an acceptable reproducibility was observed, specially when high risk tumors were being identified.

Analysis of Variance↗

Phacomatosis pigmentovascularis with a selective IgA deficiency.

We report a 1-year-old boy with an extensive cutaneous vascular malformation, oculocutaneous pigmentation, and severe neurologic abnormalities from birth, as well as a selective IgA deficiency. Ultrastructural study demonstrated prominent endothelial cells in the luminal of the blood vessels. The diagnosis of phacomatosis pigmentovascularis type IIb seemed appropriate for this patient.

Angiomatosis↗

Umbilical polyps.

We report three patients, ages 5 years, 3 years, and 4 days, with umbilical polyps. In the third child the polyp was associated with an umbilical enteric fistula. An umbilical polyp is the result of incomplete closure of the omphalomesenteric duct and becomes apparent after the umbilical cord is detached. It is a reddish tumor of a few millimeters; it seldom bleeds or is exudative. We consider it important to study every case in detail in order to exclude possible underlying embryologic anomalies such as Meckel's diverticulum and umbilical enteric fistula.

Abdominal Neoplasms↗

[Keratoderma with epidermolytic hyperkeratosis].

Three members of one family with keratoderma Thost-Unna and histopathological picture of epidermolytic hyperkeratosis are reported. Several dermatoses with this abnormality of the keratinization are mentioned and the literature cases with keratoderma are reviewed. The treatment with oral aromatic retinoid though improved the hyperkeratosis, had to be discontinued because the vulnerability of the newly skin. Exhibited erosions with the consequent discomfort. The association of keratoderma with epidermolytic hyperkeratosis would be more frequently observed if the histopathological examination were performed in all cases.

Adolescent↗

[Post-transfusion graft vs. host reaction in aplastic anemia].

The case of a 34 years old white female patient with severe bone marrow aplasia is reported. Treated with blood product transfusions, she developed cutaneous lesions consistent with graft versus host reaction. Skin biopsy revealed "satellite-cell" necrosis. The patient condition did not improve with high dose steroid therapy, and a fatal outcome was observed.

Adult↗

[Chromomycosis of the buttocks].

We report a case of chromomycosis involving buttocks in a 63 years old white male patient, who was living temporaly in several tropical areas of Argentine, due to professional reasons. The lesion had arisen 28 years ago, located in his right buttock. Clinical examination showed a large, erythematous and violaceus plaque, with atrophic center and peripheric warty nodules. Diagnosis was established on histologic and mycologic examination. Fonsecaea pedrosoi was isolated as the ethiologic agent. Treatment was instituted with oral 5-fluorocytosine and topic 5-fluorouracil with good evolution. We found our case interesting for several reasons: A) Chromomycosis is an unfrequent disease in Argentine. B) Buttock involvement is unusual. C) Clinically the patient simulated lupus vulgaris; this situation was a cause of delayed correct diagnosis and treatment.

Buttocks↗

Clinical behavior of 100 cutaneous malignant melanomas.

The last 100 patients with malignant melanoma were studied following actual methodology, with these results: mean age at diagnosis was 55.3 years; mean age at the beginning of disease was 51.8 years. Lesions were more frequent in patients with pale skin; there was no predominance of any color of eyes. Forty-nine percent of the patients were referred with a previous nevus which was confirmed only in 7%. One tumor developed on a giant pigmentary congenital nevus. Lesions showed no preponderance in one sex. Four percent of patients had multiple lesions. Familial background was found in 5%. The localization was most often to the head and neck, trunk, and legs. The most frequent types were SSMM and NMM; the first one on trunk and the second one on legs. The SSMM was observed in younger people than NMM. Level IV was seen in the greatest number of cases, with an average thickness of 3.07 mm. In SSMM, level III predominated, while in NMM, level IV predominated. The average thickness of SSMM was 1.82 mm; that of NMM was 6.25 mm. Our data are representative of malignant melanoma in Argentina. Therapy and evolution of lesions will be analyzed with an appropriate long-term follow-up.

Adolescent↗

[Reticulated pigment anomaly of the skinfolds].

We report a case of reticulate pigmented anomaly of the flexures in a 54 years-old white male patient. His lesions had developed during the last 30 years, involving neck, axillae, groins, anterior chest wall, scrotum, buttocks and thighs. The abnormality is characterized by pigmented epidermal downgrowths, with similar lesions developing around dilated pilosebaceous follicles. The condition may be compared with acanthosis nigricans. For this reason it is important to recognize this new genodermatosis in order to avoid unnecessary investigations to exclude visceral malignancy.

Acanthosis Nigricans↗

[Neurotropic melanoma].

Neurotropic melanoma is a variant of desmoplastic melanoma with a distinctive neural or Schwannian appearance of amelanotic spindled melanocytes. We report a 81 years old woman with a neurotropic melanoma on her left superciliary region. The lesion began as a lentigo maligna melanoma, Clark's level V, 4,08 mm. in thickness. The tumor relapsed on seven instances over a follow-up period of five years. Microscopic study showed a spindle cell pattern with marked neurotropism. Patient's general condition is good notwithstanding her evolution and relapses. This type of melanoma usually occurs on the face and, as we observed in our cases, exhibits a marked tendency for peripheral nerve invasion.

Aged↗

[Spiradenoma, cutaneous cylindroma and familial multiple trichoepithelioma].

Multiple spiradenoma, trichoepithelioma and traits of cylindroma in three members of a family are studied. The relationships among these tumors are discussed. Spiroadenoma and cynlindroma have shown a close interrelation. Both conditions may exist with multiple lesions in genetic autosomal dominant inherited association with multiple trichoepitelioma.

Adenoma↗

[Achromic malignant lentigo].

A case of achromic lentigo maligna is presented. The rarity and the importance of the differential diagnosis is emphasized.

Aged↗