Glucagonoma differential diagnosis: Difference between revisions

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Revision as of 14:21, 17 November 2017

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Parminder Dhingra, M.D. [2] Mohammed Abdelwahed M.D [3]

Overview

Glucagonoma must be differentiated from certain skin lesions in which necrolytic migratory erythema can be found such as acrodermatitis enteropathica, psoriasis, pellagra, and eczema. Glucagonoma should be differentiated from other causes of hyperglycemia include infection, diabetes mellitus, Cushing syndrome, renal failure, acute pancreatitis, severe stress, and prolonged fasting.

Differentiating Glucagonoma from other Diseases

Glucagonoma must be differentiated from certain skin lesions in which necrolytic migratory erythema can be found such as:^[1]

Disease	Clinical Picture			Investigations	Pictures
Disease	History	Symptoms	Signs	Investigations	Pictures
Glucagonoma^[2]^[3]^[4]^[5]	A family history of multiple endocrine neoplasia type 1	Necrolytic migratory erythema characterized by the spread of erythematous blisters and swelling across areas subject to greater friction and pressure Skin lesions involving the lower abdomen, buttocks, perineum, and groin Weight loss Glucose intolerance	Rash: Erythematous, ring shaped rash that blisters, erodes, and crusts over suggesting necrolytic migratory erythema Muscle atrophy Unilateral calf or thigh erythema and swelling Hyporeflexia Unilateral/bilateral sensory loss in the upper/lower extremity	Serum glucagon Increased plasma glucagon levels (>500 pg/mL) Concentrations above 1000 pg/mL are diagnostic of glucagonoma CT scan is used to determine: The location of the tumor Metastasis (usually liver metastasis) Appear isodense with the liver on a non-contrasted study
Pemphigus foliaceus.^[6]^[2]^[7]^[8]	Autoimmune blistering disease of the skin with characteristic lesions that are scaly, crusted erosions, often on an erythematous base.^[1] Mucosal involvement is absent even with widespread disease	Cutaneous lesion that usually develops in a seborrheic distribution The scalp, face, and trunk are common sites of involvement Skin lesions may remain localized or may coalesce to cover large areas of skin Pain or burning sensations frequently accompany the cutaneous lesions Systemic symptoms are usually absent	The skin lesions usually consist of small, scattered superficial blisters Lesions rapidly evolve into scaly, crusted erosions Positive Nikolsky sign Occasionally, pemphigus foliaceus progresses to involve the entire skin surface as an exfoliative erythroderma	Autoimmune IgG build up in the epidermis, then nearly almost all of the antibodies are aimed against desmoglein 1	Courtesy:http://www.atlasdermatologico.com.br/index.jsf
Pustular psoriasis^[2]^[3]	Positive family history of psoriasis Frequent association with histocompatibility antigen (HLA)- Cw6 A history of a long-term erythematous scaly area with ocular and joint involvement Past medical history of the patient may include Viral or bacterial infection diabetes Hypertension Chronic kidney disease Obesity.	Pain(unpleasant, superficial, sensitive, itchy, hot or burning) Pruritus High fever Dystrophic nails Recent presentation of arthralgia	Papulosquamous disease with variable morphology, distribution, severity, and course Scaling papules and plaques Koebner phenomenon: appearance of new psoriatic lesions at the site of skin injury Woronoff’s ring: ring of peripheral blanching skin around a psoriatic plaque Auspitz’s sign: Small bleeding points are seen upon disruption of a psoriatic scale	Skin biopsy Perivascular and dermal inflammatory cell infiltration Vascular dilation Absent granular layer Elongation of dermal papillae Parakeratosis Spongiform pustules of Kogoj (pathognomic of psoriasis) Munro's micro abscesses (pathognomic of psoriasis) Edema of dermal papillae Basal cell layer is expanded Leukocytosis	Courtesy:http://www.atlasdermatologico.com.br/index.jsf
Acrodermatitis enteropathica^[9]^[10]^[11]	An autosomal recessive disorder characterized by: Periorificial and acral dermatitis, alopecia, and diarrhea The genetic base is a mutation of SLC39A4 which encodes a transmembrane protein that serves as a zinc uptake protein	Symptoms appear in infants after breast milk weaning The appearance of erythematous patches and plaques of dry, scaly skin Diarrhea	Erythematous [[Patch\|patches]/plaques of dry and scaly skin The lesions may appear eczematous or may evolve into crusted vesicles, bullae or pustules The lesions are frequent in: Mouth/ perioral Anus/ Peri-anal Also involves hands, feet, and scalp Paronychia Alopecia of the scalp, eyebrows, and eyelashes	Measurement of zinc in plasma, erythrocytes, neutrophils, lymphocytes, and hair A low plasma zinc usually is defined as a value less than 60 mcg/dL The criteria for zinc deficiency are decreased zinc level in lymphocyte Depressed serum alkaline phosphatase levels	Courtesy:http://www.atlasdermatologico.com.br/index.jsf
Pellagra^[12]^[13]	It is a niacin deficiency disease characterized by photosensitive Pigmented dermatitis Diarrhea Dementia. Hisotry of: alcoholics Bariatric surgery Anorexia nervosa Malabsorptive disease Dietary deficiency especially in infants Past history of Carcinoid syndrome Prolonged use of isoniazide A family history of Hartnup disease	Photosensitivity Pigmented dermatitis in sun-exposed areas Diarrhea Dementia	Symmetric hyper pigmented rash, similar in color and distribution to a sunburn, which is present in the exposed areas of skin	Niacin status can be assessed by measuring urinary N-methylnicotinamide or by measuring the erythrocyte NAD/NADP ratio	Courtesy:http://www.atlasdermatologico.com.br/index.jsf
Chronic eczema (atopic dermatitis)	Chronic pruritic inflammatory skin disease Occurs most frequently in children but also affects adults Family history of: Atopy (Eczema Asthma Allergic rhinitis) History of dermatitis involving the skin creases Personal or family history of asthma or hay fever	Symptoms beginning in a child before the age of 2 years or, in children <4 years Dermatitis affecting the cheeks or dorsal aspect of extremities Dry skin and severe pruritus that is associated with cutaneous hyperreactivity to various environmental stimuli Exposure to: Food and inhalant allergens Irritants Infection	Visible dermatitis involving flexural surfaces Presence of generally dry skin within the past year Erythema, papulation, oozing and crusting, excoriation	Raised IgE or an eosinophilia Radioallergosorbent Test: Blood is mixed separately with many different allergens and the antibody levels measured Skin biopsy: A procedure that removes a small piece of the affected skin and sent for microscopic examination in a pathology laboratory	Courtesy:http://www.atlasdermatologico.com.br/index.jsf

Differentiating glucagonoma from other causes of hyperglycemia:

Glucagonoma can be differentiated from other causes of hyperglycemia which include:^[14]^[15]^[16]

Type1 DM

Disease	History and symptoms					Laboratory findings								Additional findings
Disease	Polyuria	Polydipsia	Polyphagia	Weight loss	Weight gain	Serum glucose	Urinary Glucose	Urine PH	Serum Sodium	Urinary Glucose	24 hrs cortisol level	C-peptide level	Serum glucagon	Additional findings
Type 1 Diabetes mellitus	✔	✔	✔	✔	-	↑	↑	Normal	Normal	N/↑	Normal	↓	Normal	Auto antibodies present (Anti GAD-65 and anti insulin anti bodies)
Type 2 Diabetes mellitus	✔	✔	✔	✔	-	↑	↑	Normal	Normal	↑	Normal	Normal	↑	Acanthosis nigricans
MODY	✔	✔	✔	-	✔	↑	↑	Normal	Normal	↑	Normal	Normal	N	-
Psychogenic polydipsia	✔	✔	-	-	-	Normal	Normal	Normal	↓	Normal	Normal	Normal	Normal	-
Diabetes insipidus	✔	✔	-	-	-	Normal	Normal	Normal	↑	Normal	Normal	Normal	Normal	-
Transient hyperglycemia	-	-	-	-	-	↑	↑	Normal	Normal	↑	Normal	Normal	N/↑	In hospitalized patients especially in ICU and CCU
Steroid therapy	✔	-	-	-	✔	↑	↑	Normal	Normal	↑	↑	N/↑	N/↑	Acanthosis nigricans,
RTA 1	-	-	-	✔	-	Normal	Normal	↑	Normal	↑	Normal	Normal	Normal	Hypokalemia, nephrolithiasis
Glucagonoma	-	-	-	-	-	↑	Normal	Normal	Normal	-	Normal	Normal	↑	Necrolytic migratory erythema
Cushing syndrome	-	-	-	-	✔	↑	-	Normal	↓	N/↑	↑	Normal	Normal	Moon face, obesity, buffalo hump, easy bruisibility

References

↑ Fang S, Li S, Cai T (2014). "Glucagonoma syndrome: a case report with focus on skin disorders". Onco Targets Ther. 7: 1449–53. doi:10.2147/OTT.S66285. PMC 4140234. PMID 25152626.
↑ Wilkinson DS (1973). "Necrolytic migratory erythema with carcinoma of the pancreas". Trans St Johns Hosp Dermatol Soc. 59 (2): 244–50. PMID 4793623.
↑ Wermers RA, Fatourechi V, Wynne AG, Kvols LK, Lloyd RV (1996). "The glucagonoma syndrome. Clinical and pathologic features in 21 patients". Medicine (Baltimore). 75 (2): 53–63. PMID 8606627.
↑ Zhang M, Xu X, Shen Y, Hu ZH, Wu LM, Zheng SS (2004). "Clinical experience in diagnosis and treatment of glucagonoma syndrome". HBPD INT. 3 (3): 473–5. PMID 15313692.
↑ Kindmark H, Sundin A, Granberg D, Dunder K, Skogseid B, Janson ET, Welin S, Oberg K, Eriksson B (2007). "Endocrine pancreatic tumors with glucagon hypersecretion: a retrospective study of 23 cases during 20 years". Med. Oncol. 24 (3): 330–7. PMID 17873310.
↑ Bystryn JC, Rudolph JL (2005). "Pemphigus". Lancet. 366 (9479): 61–73. doi:10.1016/S0140-6736(05)66829-8. PMID 15993235.
↑ Chams-Davatchi C, Valikhani M, Daneshpazhooh M, Esmaili N, Balighi K, Hallaji Z; et al. (2005). "Pemphigus: analysis of 1209 cases". Int J Dermatol. 44 (6): 470–6. doi:10.1111/j.1365-4632.2004.02501.x. PMID 15941433.
↑ Martin LK, Werth VP, Villaneuva EV, Murrell DF (2011). "A systematic review of randomized controlled trials for pemphigus vulgaris and pemphigus foliaceus". J Am Acad Dermatol. 64 (5): 903–8. doi:10.1016/j.jaad.2010.04.039. PMID 21353333.
↑ Prasad AS, Cossack ZT (1984). "Zinc supplementation and growth in sickle cell disease". Ann Intern Med. 100 (3): 367–71. PMID 6696358.
↑ Meftah S, Prasad AS, Lee DY, Brewer GJ (1991). "Ecto 5' nucleotidase (5'NT) as a sensitive indicator of human zinc deficiency". J Lab Clin Med. 118 (4): 309–16. PMID 1940572.
↑ Kiliç I, Ozalp I, Coŝkun T, Tokatli A, Emre S, Saldamli I; et al. (1998). "The effect of zinc-supplemented bread consumption on school children with asymptomatic zinc deficiency". J Pediatr Gastroenterol Nutr. 26 (2): 167–71. PMID 9481631.
↑ Prousky JE (2003). "Pellagra may be a rare secondary complication of anorexia nervosa: a systematic review of the literature". Altern Med Rev. 8 (2): 180–5. PMID 12777163.
↑ Wan P, Moat S, Anstey A (2011). "Pellagra: a review with emphasis on photosensitivity". Br J Dermatol. 164 (6): 1188–200. doi:10.1111/j.1365-2133.2010.10163.x. PMID 21128910.
↑ Barrett TG (2007). "Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered?". Pediatr Diabetes. 8 Suppl 6: 15–23. doi:10.1111/j.1399-5448.2007.00278.x. PMID 17727381.
↑ Type 1 Diabetes mellitus "Dennis Kasper, Anthony Fauci, Stephen Hauser, Dan Longo, J. Larry Jameson, Joseph Loscalzo"Harrison's Principles of Internal Medicine, 19e Accessed on December 27th,2016
↑ "namrata".

Template:WH Template:WS

[pmid25152626-1] Fang S, Li S, Cai T (2014). "Glucagonoma syndrome: a case report with focus on skin disorders". Onco Targets Ther. 7: 1449–53. doi:10.2147/OTT.S66285. PMC 4140234. PMID 25152626.

[pmid4793623-2] Wilkinson DS (1973). "Necrolytic migratory erythema with carcinoma of the pancreas". Trans St Johns Hosp Dermatol Soc. 59 (2): 244–50. PMID 4793623.

[pmid8606627-3] Wermers RA, Fatourechi V, Wynne AG, Kvols LK, Lloyd RV (1996). "The glucagonoma syndrome. Clinical and pathologic features in 21 patients". Medicine (Baltimore). 75 (2): 53–63. PMID 8606627.

[pmid15313692-4] Zhang M, Xu X, Shen Y, Hu ZH, Wu LM, Zheng SS (2004). "Clinical experience in diagnosis and treatment of glucagonoma syndrome". HBPD INT. 3 (3): 473–5. PMID 15313692.

[pmid17873310-5] Kindmark H, Sundin A, Granberg D, Dunder K, Skogseid B, Janson ET, Welin S, Oberg K, Eriksson B (2007). "Endocrine pancreatic tumors with glucagon hypersecretion: a retrospective study of 23 cases during 20 years". Med. Oncol. 24 (3): 330–7. PMID 17873310.

[pmid15993235-6] Bystryn JC, Rudolph JL (2005). "Pemphigus". Lancet. 366 (9479): 61–73. doi:10.1016/S0140-6736(05)66829-8. PMID 15993235.

[pmid159414332-7] Chams-Davatchi C, Valikhani M, Daneshpazhooh M, Esmaili N, Balighi K, Hallaji Z; et al. (2005). "Pemphigus: analysis of 1209 cases". Int J Dermatol. 44 (6): 470–6. doi:10.1111/j.1365-4632.2004.02501.x. PMID 15941433.

[pmid21353333-8] Martin LK, Werth VP, Villaneuva EV, Murrell DF (2011). "A systematic review of randomized controlled trials for pemphigus vulgaris and pemphigus foliaceus". J Am Acad Dermatol. 64 (5): 903–8. doi:10.1016/j.jaad.2010.04.039. PMID 21353333.

[pmid6696358-9] Prasad AS, Cossack ZT (1984). "Zinc supplementation and growth in sickle cell disease". Ann Intern Med. 100 (3): 367–71. PMID 6696358.

[pmid1940572-10] Meftah S, Prasad AS, Lee DY, Brewer GJ (1991). "Ecto 5' nucleotidase (5'NT) as a sensitive indicator of human zinc deficiency". J Lab Clin Med. 118 (4): 309–16. PMID 1940572.

[pmid9481631-11] Kiliç I, Ozalp I, Coŝkun T, Tokatli A, Emre S, Saldamli I; et al. (1998). "The effect of zinc-supplemented bread consumption on school children with asymptomatic zinc deficiency". J Pediatr Gastroenterol Nutr. 26 (2): 167–71. PMID 9481631.

[pmid12777163-12] Prousky JE (2003). "Pellagra may be a rare secondary complication of anorexia nervosa: a systematic review of the literature". Altern Med Rev. 8 (2): 180–5. PMID 12777163.

[pmid21128910-13] Wan P, Moat S, Anstey A (2011). "Pellagra: a review with emphasis on photosensitivity". Br J Dermatol. 164 (6): 1188–200. doi:10.1111/j.1365-2133.2010.10163.x. PMID 21128910.

[pmid17727381-14] Barrett TG (2007). "Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered?". Pediatr Diabetes. 8 Suppl 6: 15–23. doi:10.1111/j.1399-5448.2007.00278.x. PMID 17727381.

[15] Type 1 Diabetes mellitus "Dennis Kasper, Anthony Fauci, Stephen Hauser, Dan Longo, J. Larry Jameson, Joseph Loscalzo"Harrison's Principles of Internal Medicine, 19e Accessed on December 27th,2016

[16] "namrata".

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@@ Line 192: / Line 192: @@
 == Differentiating glucagonoma from other causes of hyperglycemia:==
-Glucagonoma can be differentiated from other causes of hyperglycemia which include: <ref name="pmid17727381">{{cite journal| author=Barrett TG| title=Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered? | journal=Pediatr Diabetes | year= 2007 | volume= 8 Suppl 6 | issue=  | pages= 15-23 | pmid=17727381 | doi=10.1111/j.1399-5448.2007.00278.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17727381  }}</ref><ref>Type 1 Diabetes mellitus "Dennis Kasper, Anthony Fauci, Stephen Hauser, Dan Longo, J. Larry Jameson, Joseph Loscalzo"Harrison's Principles of Internal Medicine, 19e Accessed on December 27th,2016</ref><ref>{{Cite web|url=http://www.namrata.co/diabetes-mellitus-differential-diagnosis-and-management/|title=namrata|last=|first=|date=|website=|publisher=|access-date=}}</ref>
+Glucagonoma can be differentiated from other causes of hyperglycemia which include:<ref name="pmid17727381">{{cite journal| author=Barrett TG| title=Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered? | journal=Pediatr Diabetes | year= 2007 | volume= 8 Suppl 6 | issue=  | pages= 15-23 | pmid=17727381 | doi=10.1111/j.1399-5448.2007.00278.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17727381  }}</ref><ref>Type 1 Diabetes mellitus "Dennis Kasper, Anthony Fauci, Stephen Hauser, Dan Longo, J. Larry Jameson, Joseph Loscalzo"Harrison's Principles of Internal Medicine, 19e Accessed on December 27th,2016</ref><ref>{{Cite web|url=http://www.namrata.co/diabetes-mellitus-differential-diagnosis-and-management/|title=namrata|last=|first=|date=|website=|publisher=|access-date=}}</ref>
 * [[DM1|Type1 DM]]