Acromegaly differential diagnosis: Difference between revisions

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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Prolactinoma]]  
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Prolactinoma]]  
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* On physical examination, prolactinoma demonstrates [[Visual field defect|visual field defects]] and [[diplopia]] as acromegaly.  
* On physical examination, [[prolactinoma]] demonstrates [[Visual field defect|visual field defects]] and [[diplopia]] as acromegaly.  
* On symptoms, prolactinoma patients complain of a [[headache]] as the acromegaly.   
* On symptoms, [[prolactinoma]] patients complain of a [[headache]] as the acromegaly.   
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* On physical examination, prolactinoma demonstrates [[hydrocephalus]] that distinguishes it from acromegaly.
* On physical examination, [[prolactinoma]] demonstrates [[hydrocephalus]] that distinguishes it from acromegaly.
* On symptoms, patients with prolactinoma may show [[cerebrospinal fluid]] [[rhinorrhea]].  
* On symptoms, patients with [[prolactinoma]] may show [[cerebrospinal fluid]] [[rhinorrhea]].  
* On laboratory tests, [[prolactinoma]] has a high level of [[prolactin]] that distinguishes it from acromegaly.   
* On laboratory tests, [[prolactinoma]] has a high level of [[prolactin]] that distinguishes it from acromegaly.   
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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Marfan syndrome]]
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Marfan syndrome]]
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* On physical examination, Marfan syndrome has demonstrated [[cardiac]] manifestations as the acromegaly.
* On physical examination, [[Marfan syndrome]] has demonstrated [[cardiac]] manifestations as the acromegaly.
* On physical examination, Marfan syndrome demonstrates excess linear [[bone]] growth like acromegaly.  
* On physical examination, [[Marfan syndrome]] demonstrates excess linear [[bone]] growth like acromegaly.  
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* On physical examination, Marfan syndrome patients have small [[Jaw|jaws]] that distinguish it from acromegaly.  
* On physical examination, [[Marfan syndrome]] patients have small [[Jaw|jaws]] that distinguish it from acromegaly.  
* Patients with Marfan syndrome have [[arachnodactyly]] with positive [[thumb]] and [[wrist]] signs.  
* Patients with [[Marfan syndrome]] have [[arachnodactyly]] with positive [[thumb]] and [[wrist]] signs.  
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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Precocious puberty]]
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Precocious puberty]]
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* On physical examination, excess linear bone growth is noticed like the acromegaly.  
* On physical examination, excess linear bone growth is noticed like the acromegaly.  
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* On laboratory diagnosis, precocious puberty has demonstrated high levels of [[FSH]], [[LH]], and [[testosterone]] that distinguish it from acromegaly.  
* On laboratory diagnosis, [[precocious puberty]] has demonstrated high levels of [[FSH]], [[LH]], and [[testosterone]] that distinguish it from acromegaly.  
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| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Pachydermoperiostosis]] (Primary hypertrophic osteoarthropathy)
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold; text-align:center;" |[[Pachydermoperiostosis]] (Primary hypertrophic osteoarthropathy)
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* On physical examination, pachydermoperiostosis demonstrates thickening of [[skin]] and scalp, clubbing and arthritis like acromegaly.
* On physical examination, [[pachydermoperiostosis]] demonstrates thickening of [[skin]] and [[scalp]], [[clubbing]] and [[arthritis]] like acromegaly.
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* On laboratory findings, pachydermoperiostosis has low level of the serum IGF1 which distinguishes it from acromegaly.  
* On laboratory findings, [[pachydermoperiostosis]] has low level of the serum [[IGF1]] which distinguishes it from acromegaly.  
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Revision as of 12:33, 16 August 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]

Overview

Acromegaly must be differentiated from other diseases that cause acral features like skin thickening and linear bone growth. These diseases such as Marfan syndrome, precocious puberty, prolactinoma, and pachydermoperiostosis.

Differentiating acromegaly from other Diseases

Differential Diagnosis Similar Features Differentiating Features
Prolactinoma
Marfan syndrome
Precocious puberty
  • On physical examination, excess linear bone growth is noticed like the acromegaly.
Pachydermoperiostosis (Primary hypertrophic osteoarthropathy)

References

  1. Abdullah NRA, Jason WLC, Nasruddin AB (2017). "Pachydermoperiostosis: a rare mimicker of acromegaly". Endocrinol Diabetes Metab Case Rep. 2017. doi:10.1530/EDM-17-0029. PMC 5445428. PMID 28567291.
  2. Loeys BL, Dietz HC, Braverman AC, Callewaert BL, De Backer J, Devereux RB; et al. (2010). "The revised Ghent nosology for the Marfan syndrome". J Med Genet. 47 (7): 476–85. doi:10.1136/jmg.2009.072785. PMID 20591885.
  3. Liu JK, Couldwell WT (2004). "Contemporary management of prolactinomas". Neurosurg Focus. 16 (4): E2. PMID 15191331.
  4. Papadimitriou A, Beri D, Tsialla A, Fretzayas A, Psychou F, Nicolaidou P (2006). "Early growth acceleration in girls with idiopathic precocious puberty". J Pediatr. 149 (1): 43–6. doi:10.1016/j.jpeds.2006.02.005. PMID 16860125.

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