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2.
J Thorac Cardiovasc Surg ; 86(6): 800-8, 1983 Dec.
Article in English | MEDLINE | ID: mdl-6196574

ABSTRACT

Permanent bioincorporation of a microporous tracheal prosthesis will require a stable blood supply to connective tissue supporting an epithelial surface. In experience with over 80 tracheal implants in dogs, we have observed that end-on ingrowth and epithelialization does not occur in the absence of lateral ingrowth, epithelialization is marked by the appearance of a subepithelial network of vessels, and this process must be well advanced by 6 to 8 weeks for long-term stability. These observations were extended by using microangiography to delineate the blood supply of the prosthesis/tissue complex. Six implants of bioelectric polyurethane with 10% gentamicin (3 cm length, 2 cm diameter, 1 to 1.25 mm wall thickness, 60 to 120 mu micropore diameter) were interposed in the dog thoracic trachea and wrapped with an omental pedicle. The aorta was perfused with a barium suspension at elective sacrifice between 10 weeks and 21 months. Radiographs of specimens were correlated with bronchoscopic, gross, and histopathological findings. Neovascularity of the prosthesis/tissue complex can be described in three categories: outer capsule, prosthetic wall, and inner lining. Outer capsule vessels were oriented circumferentially immediately adjacent to the prosthetic wall. They resembled arteries up to 75 mu diameter on microscopy and appeared to develop from the omentum with connections developing to the bronchial circulation. Prosthetic wall vessels up to 75 mu with thin muscular walls were noted to traverse the porous prosthetic wall. The inner lining had a network of subepithelial vessels that connected to the lamina propria vasculature of the native trachea across the anastomoses with vessels up to 120 mu in diameter. We conclude that the omentum provides an immediate blood supply and a base for early connective tissue ingrowth. Epithelialization occurs as early as 3 weeks on the favorable bed, accompanied by vascular connections to the existing lamina propria tracheal vessels. This dual organization of blood supply with connections across the prosthetic wall is probably important to long-term stability of healing.


Subject(s)
Neovascularization, Pathologic , Omentum/surgery , Polyurethanes , Prostheses and Implants , Trachea/surgery , Animals , Dogs , Epithelial Cells , Omentum/blood supply , Trachea/blood supply , Trachea/cytology
4.
Biomaterials ; 2(3): 171-6, 1981 Jul.
Article in English | MEDLINE | ID: mdl-7272407

ABSTRACT

This report describes the effects of pore size and material on soft tissue ingrowth of two medical-grade elastomers. Using the replamineform process, silicone rubber (SR) and bioelectric polyurethane (BEP) were rendered microporous with essentially the same microstructural pore configuration. Implants were prepared in each material having five pore size ranges: 18-25 microns, 30-45 microns, 75-95 microns, 60-120 microns, and 120-180 microns. Implants 1 cm X 1 cm X 1 mm were harvested at 1, 2, 4 and 12 weeks following subcutaneous implantation in mongrel dogs. Ingrowth of the 18-25 microns and 30-45 microns implants in both polymers consisted of histiocytes and dispersed fibrocytic proliferation during the first two weeks. By 12 weeks, the fibrocytic component had increased, but histiocytes remained the principal component of ingrown tissue. In contrast, initial ingrowth of the 75-95 microns, 60-120 microns and 120-180 microns implants showed increased fibrocytic proliferation and minimal histiocytic reaction. By 12 weeks, ingrowth into the larger-pore implants had progressed to broad bands of well organized collagenous stroma. Differences in the rate of tissue ingrowth were found to be related to both material and pore size. Less than 15% of the void spaces were infiltrated by 4 weeks in 18-25 microns and 30-45 microns SR implants, although this increased to approximately 50% by 12 weeks. In contrast, the 3 larger-pore SR implants and all pore sizes in the BEP implants were almost completely ingrown by 4 weeks.


Subject(s)
Biocompatible Materials , Polyurethanes , Prostheses and Implants , Silicone Elastomers , Animals , Dogs , Surface Properties
5.
Pediatrics ; 65(5): 872-80, 1980 May.
Article in English | MEDLINE | ID: mdl-7367132

ABSTRACT

In preterm infants, closure of the ductus arteriosus (DA) is often delayed, especially in those with respiratory distress syndrome (RDS). However, it has been suggested that functional closure of the DA may occur as early as 24 hours of age in some preterm infants exposed to intrauterine stress, and this is usually associated with decreased incidence of RDS. This suggests that accelerated maturation of the DA as well as of the lungs occurs in utero. Accordingly, histologic evidence of accelerated maturation of the DA was sought in a prospective autopsy study of 55 preterm infants ranging in gestational age from 19 to 32 weeks. There were four infants with clinically closed DA which showed histologic evidence of closure. The birth weight of these four infants ranged from 750--1,100 gm, the gestational age ranged from 24--32 weeks, and age of death was 39 hours to 6 days. The immediate causes of death were intracerebral hemorrhage or intrapulmonary hemorrhage, or both. Obstetric complications included chronic second trimester vaginal bleeding, abruptio placenta, malnutrition, diabetes, pulmonic stenosis of moderate degree, and chronic hypertension. These findings support the hypothesis that in some preterm infants exposed to chronic intrauterine stress, maturation of the DA is accelerated. This may result clinically in effective postnatal closure of the DA.


Subject(s)
Ductus Arteriosus/physiology , Infant, Premature, Diseases/physiopathology , Infant, Premature , Ductus Arteriosus/embryology , Ductus Arteriosus/physiopathology , Female , Fetal Distress/etiology , Fetal Distress/physiopathology , Humans , Infant, Newborn , Male , Pregnancy , Pregnancy Complications/physiopathology , Respiratory Distress Syndrome, Newborn/physiopathology
6.
Int J Dermatol ; 19(3): 149-53, 1980 Apr.
Article in English | MEDLINE | ID: mdl-7190134

ABSTRACT

The distinctions between eosinophilic fascitis (Shulman's syndrome) and scleroderma may sometimes be unclear. We describe a patient with generalized morphea who also had peripheral blood eosinophilia, fibrosis and inflammation of fascia, and hyper-globulinemia, features usually attributed to Shulman's syndrome. The latter diagnosis should be restricted to those patients whose history, clinical and laboratory findings, and response to therapy closely resemble Shulman's original description. Scleroderma and eosinophilic fasciitis may represent slightly differing aspects of the same disease spectrum, with a similar immunologic pathogenesis.


Subject(s)
Eosinophilia/pathology , Eosinophilia/veterinary , Fascia/pathology , Muscular Diseases/pathology , Myositis/veterinary , Scleroderma, Localized/pathology , Adrenal Cortex Hormones/therapeutic use , Adult , Animals , Autoimmune Diseases/complications , Humans , Male , Scleroderma, Localized/drug therapy , Skin/pathology
8.
Arch Pathol Lab Med ; 103(12): 609-12, 1979 Nov.
Article in English | MEDLINE | ID: mdl-583119

ABSTRACT

The chief cells of parathyroid adenomas were found to contain less intracytoplasmic fat than normal parathyroid glands and/or the adjacent rims of nonadenomatous parathyroid tissue. The amount of sudanophilic material in the chief cells was relatively uniform for each individual adenoma, but varied between patients. In half of the patients with parathyroid adenomas, Sudan-positive granules were generally absent from the adenomatous cells, whereas in the other half the granules were easily identifiable. The chief cells of secondary hyperplasia showed a less uniform pattern in each gland. In some areas, the stain for intracellular fat was negative, while adjacent cells contained prominent Sudan-positive granules. These findings suggest that staining frozen sections for intracellular fat is a useful but limited aid in the differentiation of parathyroid adenomas from normal parathyroid gland tissue.


Subject(s)
Adenoma/pathology , Lipid Metabolism , Parathyroid Diseases/pathology , Parathyroid Glands/pathology , Parathyroid Neoplasms/pathology , Adenoma/diagnosis , Diagnosis, Differential , Histocytochemistry , Humans , Hyperplasia , Parathyroid Diseases/diagnosis , Parathyroid Neoplasms/diagnosis
9.
J Dermatol Surg Oncol ; 5(10): 794-97, 1979 Oct.
Article in English | MEDLINE | ID: mdl-227949

ABSTRACT

Three black women were found to have granular-cell tumors on the vulva; in one, there were several additionally in other cutaneous sites. Although this benign neoplasm is uncommon on the vulva, it should be considered in the differential diagnosis of nodular lesions on the vulva. Granular-cell tumors in multiplicity occur frequently and are not a sign of metastatic disease. This lesion has predilection for blacks. Pseudocarcinomatous hyperplasia occurs typically in overlying squamous epithelium and may be misinterpreted as squamous-cell carcinoma.


Subject(s)
Neoplasms, Muscle Tissue/pathology , Vulvar Neoplasms/pathology , Adult , Black People , Carcinoma, Squamous Cell/diagnosis , Diagnosis, Differential , Female , Humans , Hyperplasia , Middle Aged , Neoplasms, Muscle Tissue/genetics , Vulvar Neoplasms/genetics
10.
Arch Dermatol ; 115(8): 969-72, 1979 Aug.
Article in English | MEDLINE | ID: mdl-464625

ABSTRACT

A lymphangiosarcoma arose at the site of a preexisting lymphangioma circumscriptum on the skin of the anterior part of the abdominal wall. To our knowledge, this is only the second such case to be reported, and in both patients, the preexisting lymphangioma circumscriptum had been exposed to substantial x-ray therapy. Since it is possible that x-irradiation may play a role in the development of this unusual malignant neoplasm, it seems advisable that lymphangioma circumscriptum not be exposed to substantial amounts of such radiation, if feasible.


Subject(s)
Lymphangioma/complications , Lymphangiosarcoma/complications , Neoplasms, Multiple Primary , Skin Neoplasms/complications , Adult , Female , Humans , Lymphangioma/pathology , Lymphangiosarcoma/pathology , Middle Aged , Skin Neoplasms/pathology
11.
Arch Dermatol ; 115(7): 862-3, 1979 Jul.
Article in English | MEDLINE | ID: mdl-453897

ABSTRACT

Sebaceous carcinoma is an uncommon cutaneous malignant neoplasm that rarely metastasizes. We report a case in which a moderately well-differentiated sebaceous carcinoma arising on the anterior aspect of the chest produced widespread visceral metastases. This unexpected clinical behavior underscores the fact that sebaceous carcinoma of the skin can sometimes be very biologically aggressive.


Subject(s)
Carcinoma/pathology , Sebaceous Gland Neoplasms/pathology , Humans , Male , Middle Aged , Neoplasm Metastasis
12.
Urology ; 14(1): 92-4, 1979 Jul.
Article in English | MEDLINE | ID: mdl-452234

ABSTRACT

A forty-three-year-old man complained of painless, firm scrotal nodules which had first appeared at age sixteen. These were diagnosed clinically as multiple epidermoid inclusion cysts and were excised. Histologically they were composed of calcified, amorphous, granular material, characteristic of idiopathic calcinosis of the scrotum. This is a rare, benign condition without any recognized underlying metabolic abnormalities. The cause of idiopathic calcinosis of the scrotum is unknown, but we believe it is due to dystrophic calcification of dartoic muscles.


Subject(s)
Calcinosis/pathology , Scrotum , Adult , Calcinosis/surgery , Humans , Male , Scrotum/pathology , Scrotum/surgery
14.
J Dermatol Surg Oncol ; 5(6): 482-3, 1979 Jun.
Article in English | MEDLINE | ID: mdl-458016

ABSTRACT

Fibrous hamartoma of infancy is a type of juvenile fibromatosis which is either present at birth or develops before two years of age. If one is not familiar with this histological pattern, it could be mistaken for a malignant mesenchymal neoplasm. We describe the characteristic clinical and microscopic features.


Subject(s)
Hamartoma/diagnosis , Soft Tissue Neoplasms/diagnosis , Diagnosis, Differential , Female , Humans , Infant
16.
Am J Med ; 66(4): 631-8, 1979 Apr.
Article in English | MEDLINE | ID: mdl-433967

ABSTRACT

Lipotropin (LPH) has been evaluated as a potential tumor marker using a sensitive beta melanocyte-stimulating hormone (beta MSH) radioimmunoassay. All 79 acetic acid extracts of carcinomas of lung, colon, stomach, esophagus and breast contained LPH in concentrations greater than blood; 61 of 79 extracts contained LPH in larger amounts than control tissues from patients without cancer. In a blind prospective study, plasma LPH was quantified in 107 patients admitted for work-up because of an abnormality on a chest roentgenogram. Thirty-one of 33 patients subsequently diagnosed as having benign lesions had plasma LPH within the 95 per cent confidence limits of normal subjects whereas 28 (36 per cent) of the 74 patients subsequently diagnosed histologically as having primary lung carcinoma had elevated levels. In control studies, 13 of 100 patients with chronic obstructive pulmonary disease had elevated plasma LPH levels; three of the 13 with elevated levels and four with normal levels have been diagnosed, during the two years of follow-up, as having lung carcinoma. In control studies of 23 patients with granulomatous lung disease, 22 had normal levels of LPH. In those with carcinoma of the colon elevated plasma LPH levels were observed in two of 21 untreated patients and in 11 of 61 patients receiving noncurative chemotherapy. Elevated plasma LPH levels were also observed in 10 of 59 patients with breast cancer, eight of 28 with pancreatic cancer, eight of 22 with gastric or esophageal cancer, six of 16 with renal cancer, four of eight with prostatic cancer, one of seven with cervical cancer and one of six with ovarian cancer. We conclude, an elevated LPH level is frequently observed in blood and tumor tissue from patients with various types of carcinoma.


Subject(s)
Hormones, Ectopic/blood , Neoplasms/blood , beta-Lipotropin/blood , Adenocarcinoma/blood , Carcinoma/blood , Colonic Neoplasms/blood , Female , Humans , Lung Diseases, Obstructive/blood , Lung Neoplasms/blood , Male , Pneumonia/blood
18.
Cutis ; 23(3): 316-8, 1979 Mar.
Article in English | MEDLINE | ID: mdl-421500

ABSTRACT

A black patient with an enlarging apocrine cystadenoma on the chest is presented herein. This location is very infrequent for this benign lesion. This is the second report of an apocrine cystadenoma in a black person.


Subject(s)
Cystadenoma/pathology , Sweat Gland Neoplasms/pathology , Adult , Humans , Male , Thorax
20.
Arch Dermatol ; 114(11): 1681-3, 1978 Nov.
Article in English | MEDLINE | ID: mdl-214043

ABSTRACT

Malignant neoplasms of the mucosa and minor salivary glands of the paranasal sinuses may involve the skin by direct extension. When a tumor appears on the overlying skin, these sinuses should be considered as a possible site of origin. Adenoid cystic carcinoma of the paranasal sinuses arise from minor salivary glands. They can infiltrate overlying skin and easily be confused with a primary cutaneous adenoid cystic carcinoma. Malignant melanomas of the paranasal sinuses are clinically very aggressive. They are often amelanotic, and this may lead to an incorrect histopathologic diagnosis. Hence, physical and radiological examination of the nose, mouth, and paranasal sinuses should be performed whenever a tumor appears in the overlying skin that does not have a clear cutaneous origin or whenever the primary site of a metastatic malignant melanoma is unknown.


Subject(s)
Carcinoma, Adenoid Cystic/pathology , Melanoma/pathology , Paranasal Sinus Neoplasms/pathology , Skin Neoplasms/pathology , Aged , Ethmoid Sinus/pathology , Female , Frontal Sinus/pathology , Humans , Male , Maxillary Sinus/pathology , Neoplasm Metastasis
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