Total Recovery from Monoclonal Gammopathy and Autoimmune Phenomena After Parathyroidectomy
Carlos A Cañas*, 1, Andrés F Echeverri1, Juan-Manuel Anaya2
Identifiers and Pagination:Year: 2012
First Page: 180
Last Page: 182
Publisher ID: TORJ-6-180
Article History:Received Date: 25/5/2012
Revision Received Date: 18/6/2012
Acceptance Date: 25/6/2012
Electronic publication date: 25/7/2012
Collection year: 2012
open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
Based on the observation of a patient with a causal relationship between hyperparathyroidism and development of both autoimmune disease and paraproteinemia, we hypothesize a novel cause of autoimmunity triggered in the context of hyperparathyroidism.
Monoclonal gammopathies have been observed in nearly 15% of the patients with Sjogrën’s syndrome (SS), a chronic autoimmune rheumatic disease characterized by salivary and lacrimal gland destruction which progresses to xerostomia and xerophthalmia related to chronic B lymphocyte activation [1,2]. There are no reports of an association between SS and primary hyperparathyroidism (PHPT) although an association between PHPT and monoclonal gammopathy has been observed , and its resolution is possible with the excision of the parathyroid adenoma [4,5]. Herein we report a patient with SS and benign monoclonal gammopathy who was diagnosed and treated for PHPT. Her autoimmune disease and paraproteinemia disappeared after resection of the parathyroid adenoma.
A 56-year-old woman was admitted due to symptomatic hypercalcemia manifested by malaise and weakness. She had previously been diagnosed for SS because of a three year history of xerostomia, xerophthalmia, dry nose, vaginal dryness, xeroderma, fatigue and arthritis in the proximal interphalangeal and metatarsophalangeal joints with the presence of positive antinuclear antibodies (ANAs), anti-Ro and anti-La antibodies, hypergammaglobulinemia as well as a biopsy of minor salivary glands disclosing focal sialodenitis a focus score of 3. Cardiopulmonary, digestive, genitourinary, or neurological symptoms were absent. She had abnormal renal function tests including increased levels of creatinine, and non-nephrotic proteinuria. A renal biopsy was done three months before admission which revealed interstitial renal disease with focal segmental glomerulosclerosis. These findings were suggestive of nephropathy associated with SS. Therefore, she was treated with 200 mg of hydroxychloroquine per day, methylprednisolone 32 mg per day, azathioprine 100 mg per day and enalapril 5 mg per day.
On admission, on physical examination, her blood pressure was 120/80 mm Hg; 70 beat per minute. Head and neck were normal. Xerophthalmia and xerostomia were present, but there was no parotid swelling or oral ulcers. Cardiopulmonary, cutaneous, neurological and osteoarticular systems were normal. General screening test was done where severe hypercalcemia and high levels of parathyroid hormone were documented (Table 1). A parathyroid scintigraphy showed a parathyroid adenoma. Serum protein electrophoresis showed a typical monoclonal band at gamma zone. The anemic state was interpreted as multifactorial: anemia of chronic disease, kidney failure and autoimmune hemolytic component. Neck surgery was performed finding a retrothyroid mass which was resected and a parathyroid adenoma was histopathologically confirmed. After two days of parathyroidectomy, the levels of calcium and parathyroid hormone turned to normal levels. Calcium and calcitriol were indicated after surgery. No hunger bone syndrome status was presented. After two months, the patient’s joint pain and sicca-symptoms improved with a significant decrease in levels of calcium, parathyroid hormone, autoantibodies and gammaglobiulins. One year later, it was possible to withdraw steroid and immunosupresive drugs. Two years later, she was asymptomatic without treatment and her laboratory exams were normal including to serum protein electrophoresis (Table 1).
Laboratory Analyses and Medical Treatment Before the Parathyroidectomy and Changes Described After Surgery
|Variable||Reference||Analysis Before Parathyroidectomy||Analysis After Parathyroidectomy||Significant Changes|
|2 months||2 years|
|White-cell count||4500-11,000 /mm3||3640||8420||7250|
|Platelet count||150-400 mm3||256.000||344.000||340.000|
|ERS ml/h||1-20 ml/ h||58||6||7||*|
|C-reactive protein||0-1 mg/dl||2.6||Negative||Negative|
|Glucose (mg/dl)||70-110 mg/dl||83||91||88|
|Urea nitrogen (mg/dl)||8-25 mg/dl||35.4||35.5||22|
|Creatinine (mg/dl)||0.6 – 1.1 mg/dl||1.9||1.92||1.1||*|
|Parathyroid hormone||10-65 pg/ml||213||82.9||34||*|
|TSH||0.4- 4 µU/ml||1.76||0.86||1.7|
|Rheumatoid factor||< 14||Negative||Negative||Negative|
|Direct coombs||Negative||Positive ++||Negative||Negative||*|
|Serum albúmine||2.9-4.9 gr/dl||4.2||3.13||4.3|
|Serum α 1 globuline||0.08-0.36 gr/dl||0.2||0.1||0,2|
|Serum α 2 globuline||0.44-1.09 gr/dl||0.84||0.65||0.9|
|Serum β 1 globuline||0.66-1.05 gr/dl||0.66||0.64||0.9|
|Serum γ globuline||0.57-1.95 gr/dl||2.1||0.32||0.89||*|
|Serum Kappa chain||574- 1276||2140||519||502||*|
|Serum lambda chain||269-632||952||263||308||*|
|Urine Kappa chain||< 1.85 mg/dl||2.59||<1.85||<1.85|
|Urine Lambda chain||< 5 mg/dl||5.2||<5||<5|
|Prednisone||25 mg/d||10 mg/d||Withdraw|
|Hydroxychloroquine||200 mg/d||100 mg/d||Withdraw|
|Azathioprine||100 mg/d||50 mg/d||Withdraw|
* Variable normalization.
** Significant decline in the variable. ESR: Erytrosedimentation rate. CRP: reactive C-protein. ALT: Alanine aminotransferase. AST: Aspartate aminotransferase. HBsAg: hepatitis B virus surface antigen. HCV: hepatitis C virus.
PHPT is associated with diverse rheumatologic manifestations, for example, osteitis, pseudogout, muscular debility and osteoporosis. The association with gammopathies has been described in medical literature as case reports. A prospective, controlled study showed a high prevalence (10%) of this association . After the removal of the parathyroid adenoma, some patients presented remission of hyperparathyroidism and gammopathy, which would suggest a causal relationship [3,4]. The most likely explanation for this phenomenon is the effect of the parathyroid hormone (PTH) on stromal cells (i.e. osteoblasts), inducing the release of interleukin-6 (IL-6), which in turn stimulates B lymphocytes for activation and differentiation of plasmocytes and the subsequent production of antibodies [6,7]. Additionally, IL-6 is produced and secreted by human parathyroids and it is probable that this production and secretion contribute directly to the elevation of its serum levels in patients with PHPT . Unfortunately, in the series it was not possible to measure serum IL-6 because this assay is not available in our country. A causal association between PHPT and autoimmune processes is theoretically likely based on humoral immunity activation. However, this condition has not been demonstrated.
IL-6 would be the most likely link between PHPT and stimulation of B lymphocytes and plasma cells which, in the current presentation, is associated with the development of gammopathy and SSP, and they improve with the treatment of PHPT. Some symptoms associated with PHPT such as fatigue and arthralgia might also be explained through various proinflammatory effects of IL-6. Recalling that, this cytokine is also produced by monocytes, macrophages, T lymphocytes, B lymphocytes, endothelial cells, etc., which stimulate other cells that trigger other biological effects .
In summary, we report a patient presenting with monoclonal gammopathy and interstitial renal disease associated with SS and HPTH. A striking improvement in clinical and laboratory aspects was observed after parathyroidectomy. To the best of our knowledge the association between PTHP and SS has not been reported previously. Further studies to understand the role of PTH in the autoimmune process are needed. This case presents a sequence of events that make us assume a form of autoimmune trigger.
CONFLICT OF INTEREST
The authors confirm that this article content has no conflicts of interest.