A case of acanthosis nigricans—an investigative approach
Identifieur interne : 006C48 ( Istex/Curation ); précédent : 006C47; suivant : 006C49A case of acanthosis nigricans—an investigative approach
Auteurs : Shernaz Walton ; Lionel Krause ; Janet MarksSource :
- Clinical and Experimental Dermatology [ 0307-6938 ] ; 1984-01.
Descripteurs français
- Wicri :
- topic : Glucose.
English descriptors
- KwdEn :
- Abdominal pain, Abnormality, Acanthosis, Acanthosis nigricans, Adenocarcinoma, Biochemical analysis, Birth rate, Cadaverine, Clinical biochemistry, Dermatology, Epidermal, Epidermal growth factor, Epidermal proliferation, Experimental dermatology, Glucagon, Glucose, Glucose load, Growth hormone, Histological, Histological appearance, Histological examination, Infirmary, Insulin, Insulin receptors, Insulin resistance, Lymph nodes, Malignant, Malignant disease, Newcastle, Nigricans, Oesophagus, Peptide, Receptor, Royal victoria infirmary, Seborrhoeic warts, Spermine, Tumour, Tyne, University department, Warty, Warty appearance, Warty skin.
- Teeft :
- Abdominal pain, Abnormality, Acanthosis, Acanthosis nigricans, Adenocarcinoma, Biochemical analysis, Birth rate, Cadaverine, Clinical biochemistry, Dermatology, Epidermal, Epidermal growth factor, Epidermal proliferation, Experimental dermatology, Glucagon, Glucose, Glucose load, Growth hormone, Histological, Histological appearance, Histological examination, Infirmary, Insulin, Insulin receptors, Insulin resistance, Lymph nodes, Malignant, Malignant disease, Newcastle, Nigricans, Oesophagus, Peptide, Receptor, Royal victoria infirmary, Seborrhoeic warts, Spermine, Tumour, Tyne, University department, Warty, Warty appearance, Warty skin.
Abstract
A patient with acanthosis nigricans secondary to a metastatic jejunal adenocarcinoma is described. An attempt was made to define the basic epidermal defect and to examine such possible influences as somatotrophin, epidermal growth factor, intestinal peptides and insulin receptors. No evidence to support a hyperproliferative epidermal mechanism was found and the hormonal profile was normal. However, there was an increase in circulating α‐MSH and this may have contributed to the pigmentation seen in this patient.
Url:
DOI: 10.1111/j.1365-2230.1984.tb00756.x
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Shernaz Walton<affiliation><mods:affiliation>Correspondence address: Dr Shernaz Walton, University Department of Dermatology, Royal Victoria Infirmary, Newcastle upon Tyne NE1 4LP.</mods:affiliation>
<wicri:noCountry code="subField">4LP.</wicri:noCountry>
</affiliation>
<affiliation><mods:affiliation>University Department of Dermatology, Royal Victoria Infirmary, Newcastle upon Tyne</mods:affiliation>
<wicri:noCountry code="subField">Tyne</wicri:noCountry>
</affiliation>
<affiliation><mods:affiliation>University Department of Dermatology, Royal Victoria Infirmary, Newcastle upon Tyne</mods:affiliation>
<wicri:noCountry code="subField">Tyne</wicri:noCountry>
</affiliation>
Le document en format XML
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<term>Abnormality</term>
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<term>Acanthosis nigricans</term>
<term>Adenocarcinoma</term>
<term>Biochemical analysis</term>
<term>Birth rate</term>
<term>Cadaverine</term>
<term>Clinical biochemistry</term>
<term>Dermatology</term>
<term>Epidermal</term>
<term>Epidermal growth factor</term>
<term>Epidermal proliferation</term>
<term>Experimental dermatology</term>
<term>Glucagon</term>
<term>Glucose</term>
<term>Glucose load</term>
<term>Growth hormone</term>
<term>Histological</term>
<term>Histological appearance</term>
<term>Histological examination</term>
<term>Infirmary</term>
<term>Insulin</term>
<term>Insulin receptors</term>
<term>Insulin resistance</term>
<term>Lymph nodes</term>
<term>Malignant</term>
<term>Malignant disease</term>
<term>Newcastle</term>
<term>Nigricans</term>
<term>Oesophagus</term>
<term>Peptide</term>
<term>Receptor</term>
<term>Royal victoria infirmary</term>
<term>Seborrhoeic warts</term>
<term>Spermine</term>
<term>Tumour</term>
<term>Tyne</term>
<term>University department</term>
<term>Warty</term>
<term>Warty appearance</term>
<term>Warty skin</term>
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<term>Abnormality</term>
<term>Acanthosis</term>
<term>Acanthosis nigricans</term>
<term>Adenocarcinoma</term>
<term>Biochemical analysis</term>
<term>Birth rate</term>
<term>Cadaverine</term>
<term>Clinical biochemistry</term>
<term>Dermatology</term>
<term>Epidermal</term>
<term>Epidermal growth factor</term>
<term>Epidermal proliferation</term>
<term>Experimental dermatology</term>
<term>Glucagon</term>
<term>Glucose</term>
<term>Glucose load</term>
<term>Growth hormone</term>
<term>Histological</term>
<term>Histological appearance</term>
<term>Histological examination</term>
<term>Infirmary</term>
<term>Insulin</term>
<term>Insulin receptors</term>
<term>Insulin resistance</term>
<term>Lymph nodes</term>
<term>Malignant</term>
<term>Malignant disease</term>
<term>Newcastle</term>
<term>Nigricans</term>
<term>Oesophagus</term>
<term>Peptide</term>
<term>Receptor</term>
<term>Royal victoria infirmary</term>
<term>Seborrhoeic warts</term>
<term>Spermine</term>
<term>Tumour</term>
<term>Tyne</term>
<term>University department</term>
<term>Warty</term>
<term>Warty appearance</term>
<term>Warty skin</term>
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<front><div type="abstract" xml:lang="en">A patient with acanthosis nigricans secondary to a metastatic jejunal adenocarcinoma is described. An attempt was made to define the basic epidermal defect and to examine such possible influences as somatotrophin, epidermal growth factor, intestinal peptides and insulin receptors. No evidence to support a hyperproliferative epidermal mechanism was found and the hormonal profile was normal. However, there was an increase in circulating α‐MSH and this may have contributed to the pigmentation seen in this patient.</div>
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