LGCmain
Indian Journal of Pathology and Microbiology
Home About us Instructions Submission Subscribe Advertise Contact e-Alerts Ahead Of Print Login 
Users Online: 643
Print this page  Email this page Bookmark this page Small font sizeDefault font sizeIncrease font size


 
  Table of Contents    
IMAGE  
Year : 2011  |  Volume : 54  |  Issue : 3  |  Page : 626-628
Ochronosis: A report of three cases and review of the literature


1 Department of Pathology, Shrimati Kashibai Navale Medical College and General Hospital, Narhe, Pune, India
2 Department of Orthopedics, Shrimati Kashibai Navale Medical College and General Hospital, Narhe, Pune, India

Click here for correspondence address and email

Date of Web Publication20-Sep-2011
 

How to cite this article:
Babanagare S V, Deshmukh S D, Khadilkar M S, Patil A A. Ochronosis: A report of three cases and review of the literature. Indian J Pathol Microbiol 2011;54:626-8

How to cite this URL:
Babanagare S V, Deshmukh S D, Khadilkar M S, Patil A A. Ochronosis: A report of three cases and review of the literature. Indian J Pathol Microbiol [serial online] 2011 [cited 2020 Nov 29];54:626-8. Available from: https://www.ijpmonline.org/text.asp?2011/54/3/626/85122


Ochronosis is the deposition of polymerized products of homogentisic acid in the connective tissues resulting in bluish black discoloration. It is one of the major manifestations of alkaptonuria, which is a rare autosomal recessive metabolic disorder characterized by deficiency of homogentisate 1,2-dioxygenase enzyme. [1] The major manifestations include the following: Urinary elimination of homogentisic acid, arthritis of large joints, deposition of pigment in soft tissues, and rarely cardiac, renal (nephrolithiasis), and ocular affliction. The joint involvement is generally clinically manifested in the third decade. [2] We encountered 3 cases of ochronosis with hip joint involvement and pigmented macules at multiple sites. The rare and interesting cases with varied manifestations have prompted us to report these cases.

Three cases of ochronosis were encountered by us over a period of 3 years at our general hospital. The details of the cases are as follows:

A 40-year-old woman presented with chronic pain in the left hip joint and history of passing dark colored urine since childhood. She also had a history of progressive bluish black pigmentation of the skin and nails [Figure 1] and [Figure 2]. Similar history was also present in 3 of her siblings. Skin involvement was noted over both hands and pinna. Roentgenogram of the spine showed extensive calcification of the intervertebral discs. Urine alkalinization showed development of black color. Diagnosis of severe ochronotic arthritis was made on the basis of the clinical and laboratory findings and the patient underwent total hip replacement surgery of both hip joints. Intraoperatively, dislocation of the left hip joint with erosion of the overlying cartilage was noted. Gross examination showed blackish discoloration of the femur head. Histopathological examination revealed a brittle fragmented cartilage with granular greyish brown pigment extracellularly as well as extracellularly within chondrocytes and synovial cells. Postoperative period followed 6 months was uneventful.

A 55-year-old man presented with chronic pain in the right hip joint, difficulty in walking and sitting cross-legged. There was no other significant medical or family history. The physical examination did not reveal pigmentation of the skin or sclera.
Figure 1: (a) Bluish black discoloration on skin and soft tissue of index fingers of both hands. (b) Similar bluish black discoloration of nail beds

Click here to view
Figure 2: Bluish black discoloration over the skin and cartilage of ear

Click here to view


A diagnosis of right hip osteoarthritis was made and total hip replacement surgery was performed. The excised femur head was subjected to histopathological examination, which revealed a blackish-brown pigment intracellularly as well as extracellularly [Figure 3]. In the light of the histopathological findings, a diagnosis of ochronosis was suspected. Urine alkalinization resulted in development of black color [Figure 4], and the diagnosis was confirmed by Benedict's test. Postoperative recovery of the patient was good. This case did not reveal involvement of any other organ.
Figure 3: (a) Excised head of femur showing black discoloration of the articular cartilage and surrounding soft tissue. (b) Photomicrograph showing granular yellowish brown pigment intracellularly and extracellularly (H and E, x100)

Click here to view
Figure 4: (a) Color of freshly passed urine; and (b) development of dark color after alkalinization

Click here to view


A 50-year-old lady was admitted with symptoms of acute gastroenteritis since 5 days. History of gradual onset skin discoloration, severe backache, and pain in both the hip joints was elicited. Physical examination revealed bluish black macules and papules over the face, forearms, hands, palms and feet, nails, and sclerae.

The results of the routine laboratory investigations were within normal limits; however, urine alkalinization and Benedict's test were positive for alkaptonuria. Magnetic resonance imaging of the lumbosacral spine showed multilevel disc calcification [Figure 5]. The histopathological findings were similar to those described in the previous cases.
Figure 5: T2-weighted sagittal magnetic resonance images of lower dorsolumbar spine revealing central intervertebral disc calcification

Click here to view


The patient was treated for acute gastroenteritis and therapy with nonsteroidal anti-inflammatory drugs (NSAIDs) and Vitamin C was started for the ochronotic arthritis. A total hip replacement surgery was advised; however, the patient was not willing for it and therefore was discharged.


   Discussion Top


Ochronosis was first described by Scribonius in 1584 in a boy whose urine was "as black as ink." The term alkaptonuria was first coined by Boedeker in 1891, as quoted by Fischer et al. [2] The term ochronosis was first used by Virchow due to the accumulation of the granular yellowish pigment in the connective tissue, which resembled ochre (yellow). [2]

One of the earliest manifestations of alkaptonuria is darkening of urine. The urine is of a normal color on voiding; however, it darkens on standing for several hours. This may not be observed due to the use of modern plumbing; hence many individuals never notice any abnormal color to their urine. [2],[3] Only one of our patients gave history of passing dark urine, thus highlighting the utility of the simple urine alkalinization test for diagnosis.

Degenerative joint disease usually develops after the third decade. Low back pain was observed in 94% of patients before the age of 40 years in one large series. [1] The knee, hip, and shoulder joints are also frequently affected. By the age of 55 years, 50% of patients required at least one joint replacement surgery. [1] In all our cases, hip arthropathy was the most troublesome symptom and necessitated total hip replacement surgery.

Discoloration of the skin is usually observed after the third decade. [2] The most commonly involved sites are the ear cartilage, eyelids, sclera, and nails. Tendons may also be involved, frequently observed as discoloration over the knuckles. Two of our patients showed significant skin discoloration. Notably one of our patients did not show any abnormal pigmentation of the skin or the sclera and diagnosis was made on the basis of intraoperative and investigation findings. Discoloration of the cartilages and tendons was noted in all three.

Reviewing the literature, ochronosis has been documented to be associated with affection of the heart in the form of valvular dystrophic calcification, aortic stenosis, and coronary disease. Some workers have reported occurrence of nephrolithiasis. Ocular manifestations in ochronosis have been reported to be mistaken for melanoma. [2] It must be mentioned that in all our cases there was absence of cardiac, renal, or ocular complications and these were ruled out by relevant investigations.

Macroscopically the tissue pigmentation varied from brown to black. Ochronotic pigment is documented to be deposited in the form of ochre colored granules in all layers of the cartilage. [4] In 2 of the 3 present cases, microscopic examination of the synovium and periarticular soft tissue showed shards of yellowish brown pigment deposits as noted by other workers. [5]

Currently there is no effective treatment for alkaptonuria and management is symptomatic. Arthropathy is usually treated with NSAIDs; however, in advanced cases, joint replacement surgery provides significant relief from symptoms.

 
   References Top

1.Phornphutkul C, Introne WJ, Perry MB, Bernardini I, Murphey MD, Fitzpatrick DL, et al. Natural history of alkaptonuria. N Engl J Med 2002;347:2111-21.  Back to cited text no. 1
[PUBMED]  [FULLTEXT]  
2.Fisher AA, Davis MW. Alkaptonuric ochronosis with aortic valve and joint replacements and femoral fracture. Clin Med Res 2004;2:209-15.  Back to cited text no. 2
[PUBMED]  [FULLTEXT]  
3.Longo N. Inherited disorders of amino acid metabolism presenting in adults. In: Braunwald E, Fauci AS, Kasper DL, Hauser SL, Longo DL, Jameson JL, editors. Harrison's Principles of Internal Medicine. 15 th ed. New York: McGraw Hill; 2001. p. 2307.  Back to cited text no. 3
    
4.Laskar FH, Sargison KD. Ochronotic arthropathy. J Bone Joint Surg 1970;52:653-66.  Back to cited text no. 4
    
5.Kruithof E, Baeten D, Veys EM, De Keyser F, Suykens S, De Wilde L, et al. Case Number 29: Ochronosis: Synovial histopathological characteristics. Ann Rheum Dis 2004;63:130.  Back to cited text no. 5
[PUBMED]  [FULLTEXT]  

Top
Correspondence Address:
S V Babanagare
Department of Pathology, Smt. Kashibai Navale Medical College and General Hospital, Narhe, Pune - 411 041
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0377-4929.85122

Rights and Permissions


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]

This article has been cited by
1 Associations rares ou trompeuses entre pathologies articulaires et pathologies ORL
Jean-Marie Berthelot
Revue du Rhumatisme Monographies. 2018; 85(4): 308
[Pubmed] | [DOI]
2 Ocronosis y osteoporosis: a propósito de un caso
Ismael Calero Paniagua,Carlos Alberto Montilla Morales,Tatiana Elizabeth Carranco Medina,María Dolores Sánchez González
Reumatología Clínica. 2015; 11(5): 330
[Pubmed] | [DOI]
3 Ochronosis and Osteoporosis: A Case Report
Ismael Calero Paniagua,Carlos Alberto Montilla Morales,Tatiana Elizabeth Carranco Medina,María Dolores Sánchez González
Reumatología Clínica (English Edition). 2015; 11(5): 330
[Pubmed] | [DOI]
4 Prostatic calcification in ochronosis
Jyoti Ranjan Parida,Durga Prasanna Misra,Pradeepta Sekhar Patro,Vikas Agarwal
Indian Journal of Rheumatology. 2014;
[Pubmed] | [DOI]
5 What is your diagnosis?
Anil Abrol,Naval Mendiratta,Pradip Prajapati,Surya Bhan,Ashok Kumar
Indian Journal of Rheumatology. 2012; 7(4): 230
[Pubmed] | [DOI]



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Email Alert *
    Add to My List *
* Registration required (free)  


   Discussion
    References
    Article Figures

 Article Access Statistics
    Viewed6770    
    Printed87    
    Emailed2    
    PDF Downloaded199    
    Comments [Add]    
    Cited by others 5    

Recommend this journal