Also known as generalized hematogenous TB, miliary TB occurs when a tuberculous lesion erodes into a blood vessel, disseminating millions of tubercle bacilli into the bloodstream and throughout the body. Uncontrolled massive dissemination can occur during primary infection or after reactivation of a latent focus. The lungs and bone marrow are most often affected, but any site may be involved.
Miliary TB is most common among
Symptoms include fever, chills, weakness, malaise, and often progressive dyspnea. Intermittent dissemination of tubercle bacilli may lead to a prolonged fever of unknown origin (FUO). Bone marrow involvement may cause anemia, thrombocytopenia, or a leukemoid reaction.
Infection of the kidneys may manifest as pyelonephritis (eg, fever, back pain, pyuria) without the usual urinary pathogens on routine culture (sterile pyuria). Infection commonly spreads to the bladder and, in men, to the prostate, seminal vesicles, or epididymis, causing an enlarging scrotal mass. Infection may spread to the perinephric space and down the psoas muscle, sometimes causing an abscess on the anterior thigh.
Salpingo-oophoritis can occur after menarche, when the fallopian tubes become vascular. Symptoms include chronic pelvic pain and sterility or ectopic pregnancy due to tubal scarring.
Meningitis often occurs in the absence of infection at other extrapulmonary sites. In the US, it is most common among the elderly and immunocompromised, but in areas where TB is common among children, TB meningitis usually occurs between birth and 5 yr. At any age, meningitis is the most serious form of TB and has high morbidity and mortality. It is the one form of TB believed to be prevented in childhood by vaccination with BCG.
Symptoms are low-grade fever, unremitting headache, nausea, and drowsiness, which may progress to stupor and coma. Kernig and Brudzinski signs may be positive. Stages are
Stroke may result from thrombosis of a major cerebral vessel. Focal neurologic symptoms suggest a tuberculoma.
Pericardial infection may develop from foci in mediastinal lymph nodes or from pleural TB. In some high-incidence parts of the world, TB pericarditis is a common cause of heart failure.
Patients may have a pericardial friction rub, pleuritic and positional chest pain, or fever. Pericardial tamponade may occur, causing dyspnea, neck vein distention, paradoxical pulse, muffled heart sounds, and possibly hypotension.
Tuberculous lymphadenitis (scrofula) typically involves the lymph nodes in the posterior cervical and supraclavicular chains. Infection in these areas is thought to be due to contiguous spread from intrathoracic lymphatics or from infection in the tonsils and adenoids. Mediastinal lymph nodes are also commonly enlarged as a part of primary pulmonary disease.
Cervical tuberculous lymphadenitis is characterized by progressive swelling of the affected nodes. In advanced cases, nodes may become inflamed and tender; the overlying skin may break down, resulting in a draining fistula.
Cutaneous tuberculosis (scrofuloderma) results from direct extension of an underlying TB focus (eg, a regional lymph node, an infected bone or joint) to the overlying skin, forming ulcers and sinus tracts.
Lupus vulgaris results from hematogenous or lymphogenous dissemination to the skin from an extracutaneous focus in a sensitized patient.
Tuberculosis verrucosa cutis (prosector's wart) occurs after exogenous direct inoculation of the mycobacteria into the skin of a previously sensitized patient who has moderate to high immunity against the bacilli.
Rarely, TB develops on abraded skin in patients with cavitary pulmonary TB.
Weight-bearing joints are most commonly involved, but bones of the wrist, hand, and elbow may also be affected, especially after injury.
Pott disease is spinal infection, which begins in a vertebral body and often spreads to adjacent vertebrae, with narrowing of the disk space between them. Untreated, the vertebrae may collapse, possibly impinging on the spinal cord. Symptoms include progressive or constant pain in involved bones and chronic or subacute arthritis (usually monoarticular). In Pott disease, spinal cord compression produces neurologic deficits, including paraplegia; paravertebral swelling may result from an abscess.
Because the entire GI mucosa resists TB invasion, infection requires prolonged exposure and enormous inocula. It is very unusual in developed countries where bovine TB is rare.
Ulcers of the mouth and oropharynx may develop from eating M. bovis–contaminated dairy products; primary lesions may also occur in the small bowel. Intestinal invasion generally causes hyperplasia and an inflammatory bowel syndrome with pain, diarrhea, obstruction, and hematochezia. It may also mimic appendicitis. Ulceration and fistulas are possible.
TB may infect the wall of a blood vessel and has even ruptured the aorta. Adrenal involvement, leading to Addison disease, formerly was common but now is rare. Tubercle bacilli may spread to tendon sheaths (tuberculous tenosynovitis) by direct extension from adjacent lesions in bone or hematogenously from any infected organ.
Testing is similar to that for pulmonary TB (see Tuberculosis (TB) : Diagnosis), including chest x-ray, TST or IGRA, and microscopic analysis (with appropriate staining) and mycobacterial cultures of affected body fluids (CSF, urine, or pleural, pericardial, or joint fluid) and tissue for mycobacteria. Nucleic acid–based testing can be done on fresh fluid or biopsy samples and on fixed tissue (eg, if TB was not suspected during a surgical procedure and cultures were not done). Blood culture results are positive in about 50% of patients with disseminated TB; such patients are often immunocompromised, often by HIV infection. However, cultures and smears of body fluids and tissues are often negative because few organisms are present; in such cases, nucleic acid amplification tests (NAAT) may be helpful.
Typically, lymphocytosis is present in body fluids. A very suggestive finding in the CSF is a glucose level < 50% of that in serum and an elevated protein level.
If all tests are negative and miliary TB is still a concern, biopsies of the bone marrow and the liver are done. If TB is highly suspected based on other features (eg, granuloma seen on biopsy, positive TST or IGRA plus unexplained lymphocytosis in pleural fluid or CSF), treatment should usually proceed despite inability to demonstrate TB organisms.
Chest x-ray and other imaging, TST, and IGRA can also provide helpful diagnostic information. Chest x-ray may show signs of primary or active TB; in miliary TB, it shows thousands of 2- to 3-mm interstitial nodules evenly distributed through both lungs.
Other imaging tests are done based on clinical findings. Abdominal or GU involvement usually requires CT or ultrasonography; renal lesions are often visible. Bone and joint involvement requires CT or MRI; MRI is preferable for spinal disease.
TST and IGRA may initially be negative, but a repeat test in a few weeks is likely to be positive. If it is not, the diagnosis of TB should be questioned or causes of anergy sought.
Drug treatment is the most important modality and follows standard regimens and principles (see Tuberculosis (TB) : First-line drugs). Six to 9 mo of therapy is probably adequate for most sites except the meninges, which require treatment for 9 to 12 mo.
Corticosteroids may help in pericarditis and meningitis (for dosing, see Other treatments).
Drug resistance is a major concern; it is increased by poor adherence, use of too few drugs, and inadequate susceptibility testing.
Surgery is required for the following:
Surgical debridement is sometimes needed in Pott disease to correct spinal deformities or to relieve cord compression if there are neurologic deficits or pain persists; fixation of the vertebral column by bone graft is required in only the most advanced cases. Surgery is usually not necessary for TB lymphadenitis except for diagnostic purposes.
Tuberculosis can spread from the lungs through the bloodstream to many sites.
Symptoms depend on the affected organ but typically include fever, malaise, and weight loss.
Diagnose based identification of bacilli in infected fluid or tissue by microscopic examination and culture and/or nucleic acid amplification tests.
Treat with multiple drugs for several months and sometimes with surgery.
Drug resistance is a major concern and is increased by poor adherence, use of too few drugs, and inadequate susceptibility testing.