Clinical-Pathological Conference Series from the Medical University of Graz
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KeywordsLymph node tuberculosis Mycobacterium tuberculosis Polyarteritis nodosa Tuberculosis drug therapy
Presentation of case
Dr. A.M. Goritschan:
The black African patient had immigrated from Lagos, Nigeria 18 months before admission to Austria to join her husband, who had immigrated to Austria 13 years earlier. Her travel history was negative since arrival in Austria; her medical history was positive for arthralgia and a skin rash 2 years earlier, when she was still living in Nigeria. These symptoms were treated with unspecified injections and oral medication for 5 days. The symptoms subsided when she became pregnant with her first child. After an unremarkable pregnancy and 4 months before the current admission she gave birth to a second healthy child. The patient attended the dermatology outpatient clinic 3 weeks before admission because of a skin rash on her back and fever. She was diagnosed with folliculitis and an ointment with a combination of betamethasone and gentamicin was prescribed for topical treatment. The rash appeared on the hands and feet of the breast feeding woman 2 weeks later with small skin lesions that exsiccated after secretion of a milky exudate. The patient reported fever, mainly during the night and some improvement with paracetamol. An enlarged firm lymph node was palpable in the left axilla. Serology for syphilis and human immunodeficiency virus (HIV) was negative, as was direct examination for scabies. The patient’s laboratory tests were notable for hemoglobin 11.7 g/dl (normal: 12.0–15.3 g/dl), hematocrit 34.8% (normal: 35.0–45.0%), alkaline phosphatase 153 U/l (normal: 35–105 U/l), gamma-glutamyl transferase (GGT) 42 U/l (normal: <38 U/l), aspartate-amino transferase (AST) 37 U/l (normal: <30 U/l), alanine aminotransferase (ALT) 49 U/l (normal: <35 U/l) and C‑reactive protein (CRP) 37.3 mg/l (normal: <5.0 mg/l). At the follow-up visit 2 weeks later the patient reported worsening of her condition. The skin rash was unchanged, but she additionally complained of pain in both lower legs, the ankles and her left foot were swollen. She still had nocturnal fever with temperatures up to 39.0 °C and there was now a second palpable, indolent lymph node in the right axilla. After one of the skin lesions on the thighs was biopsied, the patient and her 4‑month-old daughter were admitted to the department of internal medicine for further work-up.
The patient weighed 68 kg and her height was 170 cm with a body mass index (BMI) of 23.5 kg/m2, her neck was supple, her blood pressure was 112/73 mm Hg, and the heart rate was 65 per minute and regular. Except for the two palpable, axillary lymph nodes and the follicular skin rash, the patient complained of pain on firm palpation in both lower legs; both ankles and feet were slightly swollen. The rest of the physical examination was unremarkable, as were the electrocardiogram and chest radiograph. Native computed tomography (CT) of the chest revealed an enlarged lymph node (3.0 × 3.6 cm) in the right axilla. Magnetic resonance imaging (MRI) of the mediastinum was unremarkable, but showed several enlarged lymph nodes in the right axilla with a maximum diameter of 3.6 cm. Lymph nodes in the left axilla were up to 8 mm in diameter. Urinalysis and urinary sediment were within normal limits. At this time the patient’s laboratory tests were notable for CRP 63 mg/l (normal: <5 mg/l), erythrocyte sedimentation rate 86 mm (normal: <20 mm), total protein 7.9 g/dl (normal: 6–8 g/dl), alpha-1-globulin 3.7% (normal: 1.5–3.5%), gammaglobulin 24.3% (10–18.5%) and haptoglobin 3.75 g/l (normal: 0.3–2.0 g/l). The histopathological findings for the skin biopsy showed vasculitis suggesting polyarteritis nodosa but there was no evidence of acute generalized exanthemic pustulous dermatitis (AGEP). Immunopathological parameters were negative; these included antinuclear antibodies (ANA), antineutrophil cytoplasmic antibodies against myeloperoxidase (ANCA-MPO) and proteinase 3 (ANCA-Pr3), antibodies against double-stranded DNA, mitochondria, smooth muscle cells and basal membrane, and screening for extractable nuclear antigens (ENA). At this time, treatment with prednisolone (75 mg daily) was commenced. Consequently, nocturnal fever with recent temperatures up to 40.1 °C disappeared and CRP decreased to 1 mg/l. A blood culture obtained during the night when the patient’s temperature was highest was negative. Serological tests for Borrelia burgdorferi, Bartonella henselae, Yersinia Types 3 and 9, Toxoplasma gondii, Chlamydia trachomatis, Mycoplasma pneumoniae, Epstein-Barr virus, Coxsackie A and B viruses, cytomegaly virus, enterovirus, human herpes virus, mumps and parvovirus B 19 were all negative or normal. Angiotensin-converting enzyme (ACE) was also normal. Repeated measurements of procalcitonin did not exceed 0.05 ng/ml (normal 0.03–0.05 ng/ml). Fluorescence-activated cell sorting (FACS) did not indicate a clonal cell population or cells with aberrant expression of markers on leukocytes in the peripheral blood.
A diagnostic test was performed.
Dr. B. Schneeweiss:
In essence, the patient under discussion suffers from fever 3 months postpartum, has a skin rash first diagnosed as folliculitis, which presents with small skin lesions drying up after secretion of a milky exudate. In a second phase of the disease the skin manifestations spread over the whole body and the patient developed pain on firm palpation in both lower legs; the ankles and feet were swollen. According to the protocol, the rash was not diagnosed as erythema nodosum. Administration of prednisolone markedly improved her symptoms, a response that could point to a rheumatological disease. This was, however, not confirmed by laboratory data, which were only notable for elevated CRP, blood sedimentation rate and gammaglobulin, and revealed discrete anemia and slightly increased transaminases. Several immunological parameters and screening for ENA were negative, as were ACE, blood cultures and serological tests for various infections. The histopathological findings of the skin biopsy revealed vasculitis and polyarteritis nodosa was suspected. Since the skin lesions were described to secrete milky exudate, Sweet’s syndrome should also be considered in this case.
Furthermore, it is of utmost importance to address the patient’s axillary lymphadenopathy. Depending on the size and localization of the enlarged lymph nodes, different diagnoses should be considered. Various sonographic criteria are available to distinguish benign from malignant lymphadenopathy [1, 2]. Usually, lymphadenopathy is classified as benign if lymph nodes have a diameter <1 cm and infectious and systemic diseases can be excluded. Lymph nodes with a diameter >2 cm often suggest malignancy; however, regardless of the size, the underlying cause of a progression in size of lymph nodes should always be investigated.
Causes for lymphadenopathy combined with a skin rash as described in the patient
Vesicular, bullous rash
Systemic lupus erythematosus
Inflammatory bowel disease
Systemic lupus erythematosus
Inflammatory bowel disease
Subacute bacterial endocarditis
Dr. B. Schneeweiss’s diagnosis
Discussion of case
Dr. A. Aigelsreiter:
Dr. G.J. Krejs:
Dr. Flick is a specialist for tuberculosis and will present the course of the disease in this patient.
Dr. H. Flick:
On firm diagnosis of lymph node tuberculosis, the patient received standard treatment for tuberculosis with quadruple drug therapy (rifampicin 600 mg q.d., isoniazid 300 mg q.d., pyrazinamide 1500 mg q.d., ethambutol 1000 mg q.d.) for 2 months and a 2-drug therapy (rifampicin 600 mg q.d., isoniazid 300 mg q.d.) for an additional 4 months. Prednisolone was tapered but had to be reintroduced (50 mg per day) because her vasculitis had worsened. After 2 months of treatment for tuberculosis, CT showed that the enlarged axillary lymph nodes were now much smaller. The patient became completely free of symptoms and had gained weight under long-term therapy with prednisolone. Currently, she is still under two-drug therapy for tuberculosis and additionally receives corticosteroids, which will be slowly tapered during the next months.
Dr. G.J. Krejs:
Therapy with corticosteroids in tuberculosis is considered dangerous and is usually avoided because it could trigger spread of the infection.
Dr. B. Schneeweiss:
To my knowledge, in addition to the tuberculostatic therapy, patients with tuberculous meningitis are also treated with corticosteroids despite the infection with Mycobacterium tuberculosis. In this case, however, the remarkably quick and positive response of the patient to corticosteroids is a surprising and interesting observation.
Dr. R. Hofmann-Wellenhof:
Dr. G.J. Krejs:
Since the patient complained of swollen and painful ankles, a rheumatologist was consulted.
Dr. H.-P. Brezinsek:
Diagnosis of a rheumatological disease was quite difficult because the patient had already been under corticosteroid therapy and the ankle pain as well as the painful skin rash had subsided when I examined her. Basically, tuberculosis can also affect joints, especially the spine, hips and knees, but these structures were not affected. In suspected cases, joint puncture and PCR testing for Mycobacterium tuberculosis of the punctate should be performed to confirm a joint affection by tuberculosis. Involvement of the ankle joints and even the described course of the joint symptoms in this patient would have been very atypical for tuberculosis, so that it seems very unlikely that the joint problems were indeed due to tuberculosis; they are more compatible with sarcoidosis, e. g. Löfgren’s syndrome, but this syndrome also includes erythema nodosum, which this patient did not have. Because of the rapid response to the treatment, we concluded that the symptoms were parainfectious. Unfortunately, no imaging studies (ultrasound or MRI) of her joints were made before corticosteroids were started. We can only speculate as to whether her symptoms were just arthralgia, commonly seen during infections, or arthritis. Reactive arthritis would be unlikely since the main criteria for diagnosis , e. g. enteritis and urethritis, were not present.
Dr. G.J. Krejs:
Despite advances in diagnosis and therapy, tuberculosis is still one of the world’s biggest health threats and a major public health concern; decades ago the World Health Organization established a global tuberculosis monitoring system . It is of interest that in western countries, while the total incidence of tuberculosis decreased, the proportion of extrapulmonary tuberculosis increased from 8% in 1962 to 21% in 2015 [11, 16, 17, 18]. The most common type of extrapulmonary tuberculosis is lymph node tuberculosis followed by pleural, genitourinary, bone/joint, miliary, meningeal and peritoneal manifestation of the disease .
Dr. Flick will provide further epidemiological data on tuberculosis, specifically focusing on the situation in Austria.
Dr. H. Flick:
According to the national reference center for tuberculosis, the total number of cases in Austria decreased from 1480 cases in 1997 to 582 in 2014, for a yearly incidence of 6.8 per 100,000 population. As in other high-income countries, the incidence of tuberculosis is generally higher in foreign-born persons (31.2 per 100,000 population in 2014) than in Austrian-born persons (3.3 per 100,000 population in 2014), with 82% presenting with pulmonary tuberculosis and 18% with extrapulmonary manifestations . The linear decrease of tuberculosis incidence in Austria (‑0.65 per 100,000 population per year from 1997 to 2014) is attributable to a reduction of cases in native-born persons; the incidence in foreign-born persons in Austria tends to decrease only very slightly, and is still more than ten-fold higher than in native-born persons. This discrepancy in the incidence of tuberculosis among native-born and foreign-born persons may be explained by the fact that in Austria transmission of tuberculosis is effectively limited by immediate isolation of infected patients. This is important because each case of active tuberculosis is estimated to cause 10–20 further infections . In contrast, detection of active tuberculosis and isolation of infected patients is not routine practice in many low-income countries with lower health care standards. Depending on the intensity of exposure to Mycobacterium tuberculosis, up to 30% of individuals are estimated to develop latent infection after contact with an infectious index patient  and one third of the world’s population is estimated to be latently infected with Mycobacterium tuberculosis . These individuals carry a 5–10% lifetime risk of progressing to active tuberculosis . Treatment of latent infections with isoniazid reduces the risk of future disease by 75–90% . Undetected tuberculosis (active and latent) is a major problem in low-income countries and flight and migration of people from countries with high tuberculosis incidence may additionally enhance the risk of transmission among immigrants.
If a foreign-born patient (particularly from high incidence regions such as Asia and Africa) presents with fever and unclear symptoms, tuberculosis should be suspected. The discussed patient came from Nigeria, where the yearly incidence of tuberculosis is about 300–499 per 100,000 population . Physicians should be aware of tuberculosis, particularly when clinical symptoms, travel history or migration strongly suggest the disease. When tuberculosis is suspected, a tissue biopsy should be examined with acid-fast bacilli staining, culture, and PCR, as was done in this case.
For the diagnosis of tuberculosis, it should be borne in mind that both the tuberculin skin test (TST) and interferon gamma release assay (IGRA) have highly variable sensitivity, even in active cases of tuberculosis. In patients with culture-confirmed tuberculosis, the sensitivity of the TST ranges from 75–90%; however, cross-reactivity of the intradermally injected purified protein derivate of Mycobacterium bovis with nontuberculous mycobacteria and the bacillus Calmette Guérin vaccine limits the specificity of the test in a population . It has further been shown that TST is negative in up to half of all cases of disseminated tuberculosis . The IGRA measures interferon gamma response of the immune system to infection in blood samples using highly specific Mycobacterium tuberculosis antigens, thus providing improved specificity over TST [27, 28]. However, IGRA lacks the sensitivity that is routinely demanded from other laboratory tests; false negative test results are reported in up to 25% of cases . Both TST and IGRA do not provide information on whether the disease is active or latent and a negative test does not exclude tuberculosis. False negative results may delay the correct diagnosis and treatment because physicians will probably want to rule out infection with Mycobacterium tuberculosis early and then search for other causes of disease. In this patient the IGRA was first negative and later, after the diagnosis was already established, became positive.
As observed here, immunological reactions and vasculitis in various organs are very rare, but well described. Depending on the affected organ, this can cause severe health problems in tuberculosis, especially when the central nervous system (CNS) is involved. To reduce the risk of increased immune reactions leading to vasculitis, concurrent therapy with anti-tuberculous drugs and corticosteroids is recommended in CNS tuberculosis [29, 30]. In other cases of tuberculosis, administration of corticosteroids is, however, controversial because it may worsen the response to tuberculosis therapy due to the modulation of immune reactions.
Dr. G.J. Krejs:
Dr. Harnoncourt as a pulmonologist will briefly report his experience with tuberculosis.
Dr. K. Harnoncourt:
This case reminds me of a 65-year-old nun with lymph node tuberculosis whom I treated almost 60 years ago. She presented with an enlarged lymph node and poor general health. Since tuberculosis was suspected, a lymph node biopsy was tested for Mycobacterium tuberculosis. Back then this was done in animals, i. e. mice were inoculated with material obtained from the patient. Approximately 6 weeks later this “bioassay” proved Mycobacterium tuberculosis infection in our patient. In the 1950s patients received a two-drug antituberculous standard therapy (isoniazid and streptomycin) for 6 months with a reduction in dosage after 4 months.
Dr. A. Rosenkranz:
As already mentioned, extrapulmonary tuberculosis generally carries little risk for transmission. In this case, even breastfeeding did not transmit the disease to the baby, which was tested after the mother’s diagnosis had been established. Under quadruple antituberculous therapy, however, the baby had to be weaned. Regarding the risk of transmission, I would like to mention that normal serum procalcitonin levels as observed in our patient rather suggest an immunological than an infectious cause of her symptoms .
Dr. G.J. Krejs:
In 2017 tuberculosis remains an important diagnostic consideration. In the 30-year-history of our clinical-pathological conference (CPC) series from the Medical University of Graz, including this case we discussed a total of 5 cases of tuberculosis, or 3% of all CPCs. There were two cases of tuberculous peritonitis, one of tuberculous spondylodiscitis, one of ileocecal tuberculosis, and the current patient, who suffered from lymph node tuberculosis.
Dr. B. Schneeweiss:
This case clearly highlights that even in 2017 tuberculosis should be considered when a patient presents with fever and unclear symptoms, particularly when coming from a country in which the disease is endemic.
Lymph node tuberculosis, tuberculosis-associated vasculitis mimicking polyarteritis nodosa.
The authors express their sincere gratitude to Eugenia Lamont for language editing of the manuscript.
Open access funding provided by Medical University of Graz.
Conflict of interest
E. Fabian, B. Schneeweiss, T. Valentin, H. Flick, A. Aigelsreiter, R. Hofmann-Wellenhof, L. Cerroni, A.M. Goritschan, H.-P. Brezinsek, S. Zitta, A. Rosenkranz, W. Graninger, and G.J. Krejs declare that they have no competing interests.
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