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Miliary tuberculosis

From Wikipedia, the free encyclopedia
Miliary tuberculosis
Other namesDisseminated tuberculosis, tuberculosis cutis acuta generalisata, tuberculosis cutis disseminata[1]
Chest X ray showing miliary tuberculosis
SpecialtyInfectious disease

Miliary tuberculosis is a form of tuberculosis that is characterized by a wide dissemination into the human body and by the tiny size of the lesions (1–5 mm). Its name comes from a distinctive pattern seen on a chest radiograph of many tiny spots distributed throughout the lung fields with the appearance similar to millet seeds—thus the term "miliary" tuberculosis. Miliary TB may infect any number of organs, including the lungs, liver, and spleen.[2] Miliary tuberculosis is present in about 2% of all reported cases of tuberculosis and accounts for up to 20% of all extra-pulmonary tuberculosis cases.[3]

Signs and symptoms

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Patients with miliary tuberculosis often experience non-specific signs, such as coughing and enlarged lymph nodes. Miliary tuberculosis can also present with enlarged liver (40% of cases), enlarged spleen (15%), inflammation of the pancreas (<5%), and multiple organ dysfunction with adrenal insufficiency (adrenal glands do not produce enough steroid hormones to regulate organ function).[2] Stool may also be diarrheal in nature and appearance.[citation needed]

Other symptoms include fever, hypercalcemia, choroidal tubercles, and cutaneous lesions. Firstly, many patients can experience a fever lasting several weeks with daily spikes in morning temperatures.[4]

Secondly, hypercalcemia prevails in 16–51% of tuberculosis cases.[5] It is thought that hypercalcemia occurs as a response to increased macrophage activity in the body. Such that, 1,25 dihydroxycholecalciferol (also referred to as calcitriol) improves the ability of macrophages to kill bacteria; however, higher levels of calcitriol lead to higher calcium levels, and thus hypercalcemia in some cases.[6] Thus, hypercalcemia proves to be an important symptom of miliary tuberculosis.[6]

Thirdly, chorodial tubercules, pale lesions on the optic nerve, typically indicate miliary tuberculosis in children. These lesions may occur in one eye or both; the number of lesions varies between patients.[7] Chorodial tubercules may serve as important symptoms of miliary tuberculosis, since their presence can often confirm suspected diagnosis.[8]

Lastly, 10–30% of adults and 20–40% of children with miliary tuberculosis have tuberculosis meningitis.[4] This relationship results from mycobacteria from miliary tuberculosis spreading to the brain and the subarachnoid space; as a result, leading to tuberculosis meningitis.[9]

The risk factors for contracting miliary tuberculosis are being in direct contact with a person who has it, living in unsanitary conditions, and poor nutrition. In the U.S., risk factors for contracting the disease include homelessness and HIV/AIDS.[10]

Cause

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Miliary tuberculosis is a form of tuberculosis that is the result of Mycobacterium tuberculosis travelling to extrapulmonary organs, such as the liver, spleen and kidneys.[11] Although it is well understood that the bacteria spread from the pulmonary system to the lymphatic system and eventually the blood stream, the mechanism by which this occurs is not well understood.[12]

One proposed mechanism is that tuberculous infection in the lungs results in erosion of the epithelial layer of alveolar cells and the spread of infection into a pulmonary vein.[12][13] Once the bacteria reach the left side of the heart and enter the systemic circulation, they may multiply and infect extrapulmonary organs.[13] Once infected, the cell-mediated immune response is activated. The infected sites become surrounded by macrophages, which form granuloma, giving the typical appearance of miliary tuberculosis.[14]

Alternatively, the bacteria may attack the cells lining the alveoli and enter the lymph node(s).[12] The bacteria then drain into a systemic vein and eventually reach the right side of the heart. From the right side of the heart, the bacteria may seed—or re-seed as the case may be—the lungs, causing the eponymous "miliary" appearance.[citation needed]

Diagnosis

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Tuberculosis of the lungs
Tuberculosis of the lungs

Testing for miliary tuberculosis is conducted in a similar manner as for other forms of tuberculosis, although a number of tests must be conducted on a patient to confirm diagnosis.[4] Tests include chest x-ray, sputum culture, bronchoscopy, open lung biopsy, head CT/MRI, blood cultures, fundoscopy, and electrocardiography.[10] The tuberculosis (TB) blood test, also called an Interferon Gamma Release Assay or IGRA, is a way to diagnose latent TB. A variety of neurological complications have been noted in miliary tuberculosis patients—tuberculous meningitis and cerebral tuberculomas being the most frequent. However, a majority of patients improve following antituberculous treatment. Rarely lymphangitic spread of lung cancer could mimic miliary pattern of tuberculosis on regular chest X-ray. [15]

The tuberculin skin test, commonly used for detection of other forms of tuberculosis, is not useful in the detection of miliary tuberculosis. The tuberculin skin test fails due to the high numbers of false negatives.[16] These false negatives may occur because of higher rates of tuberculin anergy compared to other forms of tuberculosis.[4]

A case of miliary tuberculosis in an 82-year-old woman:

  • X-ray, 13 days after onset, showing bilateral interstitial infiltrates
    X-ray, 13 days after onset, showing bilateral interstitial infiltrates
  • CT, 16 days after onset, showing extensive pulmonary parenchymal involvement consisting of irregular septal thickenings with ground-glass areas and centrilobular nodules with a peri-lymphatic distribution
    CT, 16 days after onset, showing extensive pulmonary parenchymal involvement consisting of irregular septal thickenings with ground-glass areas and centrilobular nodules with a peri-lymphatic distribution
  • X-ray, 22 days after onset, showing extensive bilateral reticulo-nodular infiltrates
    X-ray, 22 days after onset, showing extensive bilateral reticulo-nodular infiltrates
  • Gross pathology of the lung, spleen and kidney, showing micronodules (1–4 mm in diameter) which resemble millet seeds
    Gross pathology of the lung, spleen and kidney, showing micronodules (1–4 mm in diameter) which resemble millet seeds
  • Histopathology, showing epithelioid granulomas with multinucleated giant cells and acid-fast bacilli
    Histopathology, showing epithelioid granulomas with multinucleated giant cells and acid-fast bacilli

Treatment

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Main article: Tuberculosis treatment

The standard treatment recommended by the WHO is with isoniazid and rifampicin for six months, as well as ethambutol and pyrazinamide for the first two months. If there is evidence of meningitis, then treatment is extended to twelve months. The U.S. guidelines recommend nine months' treatment.[17] "Common medication side effects a patient may have such as inflammation of the liver if a patient is taking pyrazinamide, rifampin, and isoniazid. A patient may also have drug resistance to medication, relapse, respiratory failure, and acute respiratory distress syndrome."[10]

Prognosis

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If left untreated, miliary tuberculosis is almost always fatal. Although most cases of miliary tuberculosis are treatable, the mortality rate among children with miliary tuberculosis remains 15–20% and for adults 25–30%.[11] One of the main causes for these high mortality rates includes late detection of disease caused by non-specific symptoms.[8] Non-specific symptoms include: coughing, weight loss, or organ dysfunction.[3] These symptoms may be implicated in numerous disorders, thus delaying diagnosis. Misdiagnosis with tuberculosis meningitis is also a common occurrence when patients are tested for tuberculosis, since the two forms of tuberculosis have high rates of co-occurrence.[11]

History

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John Jacob Manget described a form of disseminated tuberculosis in 1700 and expressed its resemblance to numerous millet seeds in size and appearance and coined the term from Latin word miliarius, meaning related to millet seed.[18]

See also

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References

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  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. Chapter 74. ISBN 978-1-4160-2999-1.
  2. ^ a b Miliary Tuberculosis at eMedicine
  3. ^ a b Ray, Sayantan; Talukdar, Arunansu; Kundu, Supratip; Khanra, Dibbendhu; Sonthalia, Nikhil (2013). "Diagnosis and management of miliary tuberculosis: current state and future perspectives". Therapeutics and Clinical Risk Management. 9: 9–26. doi:10.2147/TCRM.S29179. PMC 3544391. PMID 23326198. (Retracted, see doi:10.2147/TCRM.S96338, PMID 26445545,  Retraction Watch. If this is an intentional citation to a retracted paper, please replace {{retracted|...}} with {{retracted|...|intentional=yes}}.)
  4. ^ a b c d Sharma, Surendra K.; Mohan, Alladi; Sharma, Abhishek (May 2012). "Challenges in the diagnosis & treatment of miliary tuberculosis". The Indian Journal of Medical Research. 135 (5): 703–730. ISSN 0971-5916. PMC 3401706. PMID 22771605.
  5. ^ Ko, Y-C.; Lee, C-T.; Cheng, Y-F.; Hung, K-H.; Kuo, C-Y.; Huang, C-C.; Chen, J-B. (2004-07-21). "Hypercalcaemia and haemophagocytic syndrome: rare concurrent presentations of disseminated tuberculosis in a dialysis patient: Hypercalcaemia and Haemophagocytic Syndrome". International Journal of Clinical Practice. 58 (7): 723–725. doi:10.1111/j.1368-5031.2004.00054.x. PMID 15311732.
  6. ^ a b Soofi, A., Malik, A., Khan, J., & Muzzafer, S. (2004). Severe Hypercalcemia in Tuberculosis. J Pak Med Assoc, 54(4), 213–215.
  7. ^ Rodin, Frank H.; Dickey, Lloyd B. (June 1928). "Tubercle of the Choroid in Miliary Tuberculosis: Case Report". California and Western Medicine. 28 (6): 807–809. ISSN 0093-4038. PMC 1655892. PMID 18740728.
  8. ^ a b Sahn, Steven A.; Neff, Thomas A. (April 1974). "Miliary tuberculosis". The American Journal of Medicine. 56 (4): 495–505. doi:10.1016/0002-9343(74)90482-3. PMID 4206484.
  9. ^ Donald, P; Schaaf, H; Schoeman, J (April 2005). "Tuberculous meningitis and miliary tuberculosis: the Rich focus revisited". Journal of Infection. 50 (3): 193–195. doi:10.1016/j.jinf.2004.02.010. PMID 15780412.
  10. ^ a b c MedlinePlus Encyclopedia: Disseminated tuberculosis
  11. ^ a b c Sharma, Surendra Kumar; Mohan, Alladi; Sharma, Anju; Mitra, Dipendra Kumar (July 2005). "Miliary tuberculosis: new insights into an old disease". The Lancet Infectious Diseases. 5 (7): 415–430. doi:10.1016/S1473-3099(05)70163-8. PMID 15978528.
  12. ^ a b c Krishnan, Nitya; Robertson, Brian D.; Thwaites, Guy (November 2010). "The mechanisms and consequences of the extra-pulmonary dissemination of Mycobacterium tuberculosis". Tuberculosis. 90 (6): 361–366. doi:10.1016/j.tube.2010.08.005. PMID 20829117.
  13. ^ a b Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; & Mitchell, Richard N. (2007). Robbins Basic Pathology (8th ed.). Saunders Elsevier. pp. 516–522 ISBN 978-1-4160-2973-1
  14. ^ Al Jumaah, Suliman (2012). "Tuberculosis". In Elzouki, Abdelaziz Y.; Harfi, Harb A.; Nazer, Hisham M.; Stapleton, F. Bruder; Oh, William; Whitley, Richard J. (eds.). Textbook of Clinical Pediatrics. Berlin, Heidelberg: Springer Berlin Heidelberg. pp. 1053–1059. doi:10.1007/978-3-642-02202-9_95. ISBN 978-3-642-02201-2.
  15. ^ Furqan, M; Butler, J (2010). "Miliary pattern on chest radiography: TB or not TB?". Mayo Clinic Proceedings. 85 (2): 108. doi:10.4065/mcp.2009.0523. PMC 2813816. PMID 20118384.
  16. ^ Lee, Y.-M.; Park, K.-H.; Kim, S.-M.; Park, S. J.; Lee, S.-O.; Choi, S.-H.; Kim, Y. S.; Woo, J. H.; Kim, S.-H. (December 2013). "Risk factors for false-negative results of T-SPOT.TB and tuberculin skin test in extrapulmonary tuberculosis". Infection. 41 (6): 1089–1095. doi:10.1007/s15010-013-0478-z. ISSN 0300-8126. PMID 23943073.
  17. ^ American Thoracic Society, CDC, and Infectious Diseases Society of America (June 20, 2003). "Treatment of Tuberculosis".{{cite web}}: CS1 maint: multiple names: authors list (link)
  18. ^ Manget, JJ (1700). Sepulcretum size anatomia practica. Vol. 1 (Observatio XLVII (3 vols) ed.). London: Cramer and Perrachon.

Further reading

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