Mayo Clin Proc, February 2002, Vol 77 Residents’ Clinic 189
Mayo Clin Proc. 2002;77:189-192 189 © 2002 Mayo Foundation for Medical Education and Research
Residents' Clinic
58-Year-Old Man With Fatigue and Flank Pain
GRACE KHO DY, MD,* AND ELAINE B. YORK, MD†
* Resident in Internal Medicine, Mayo Graduate School of Medicine,
Mayo Clinic, Rochester, Minn.
† Adviser to resident and Consultant in Community Internal Medi-
cine, Mayo Clinic, Rochester, Minn.
See end of article for correct answers to questions.
Address reprint requests and correspondence to Elaine B. York,
MD, Division of Community Internal Medicine, Mayo Clinic, 200 First
St SW, Rochester, MN 55905 (e-mail: york.elaine@mayo.edu).
A
58-year-old man presented to our institution because
of a 2-week history of fatigue, malaise, and lower
extremity myalgias associated with bilateral flank pain and
passage of sandy material on micturition. He denied having
fever, hematuria, nausea, vomiting, or weight loss.
The patient’s medical history was notable for recurrent
nephrolithiasis for which hydrochlorothiazide was pre-
scribed and psoriasis, which was well controlled with
Goeckerman treatment. Surgical history included nasal
polypectomy and orchiopexy for cryptorchidism.
The patient’s vital signs on admission included a tem-
perature of 37.4°C, regular heart rate of 78 beats/min, and
blood pressure of 153/83 mm Hg. Physical examination
findings were unremarkable except for multiple scaly
plaques distributed primarily on the extensor surfaces of
his knees and elbows, consistent with psoriasis. He had no
palpable lymphadenopathy or hepatosplenomegaly. The
initial complete blood cell count showed a hemoglobin
level of 11.9 g/dL (reference range shown parentheti-
cally) (13.5-17.5 g/dL), hematocrit of 33.6% (38.8%-
50%), mean corpuscular volume of 89.2 fL (81.2-95 fL),
leukocyte count of 6.9 × 10
9
/L (3.5-10.5 × 10
9
/L), and
platelet count of 266 × 10
9
/L (150-450 × 10
9
/L). Labora-
tory studies yielded the following: sodium, 136 mEq/L
(135-145 mEq/L); potassium, 4.3 mEq/L (3.6-4.8 mEq/
L); calcium, 12.5 mg/dL (8.9-10.1 mg/dL); magnesium,
1.5 mg/dL (1.7-2.1 mg/dL); creatinine, 4.6 mg/dL (0.8-
1.2 mg/dL); serum urea nitrogen, 42 mg/dL (6-21 mg/
dL); chloride, 96 mEq/L (100-108 mEq/L); bicarbonate,
29 mEq/L (22-29 mEq/L); phosphorus, 3.7 mg/dL (2.5-
4.5 mg/dL); and serum pH, 7.46 (7.35-7.45). Urinalysis
revealed a pH of 6.5 and a trace of proteinuria; micro-
scopic examination showed 1 to 3 red blood cells per
high-power field. Findings on chest radiography were
normal except for minimal anterior wedging of 1 mid-
thoracic vertebral body. The patient was admitted to the
hospital for management of hypercalcemia.
1. Which one of the following is the most likely cause of
hypercalcemia in this patient?
a. Primary hyperparathyroidism
b. Hydrochlorothiazide intake
c. Hyperthyroidism
d. Multiple myeloma (MM)
e. Familial hypocalciuric hypercalcemia (FHH)
The degree of hypercalcemia may be useful diagnosti-
cally. Primary hyperparathyroidism is often associated
with borderline or mild hypercalcemia, with the serum
calcium concentration often being lower than 11 mg/dL.
1
Anemia is not typically present, although it may occur
occasionally due to replacement of the marrow with fibro-
sis. These features do not fit our patient’s clinical situation.
In a patient taking hydrochlorothiazide, thiazide-in-
duced hypercalcemia is usually mild. Thus, thiazide intake
per se is rarely the primary cause of a serum calcium level
higher than 12 mg/dL. Our patient’s calcium level suggests
the presence of an underlying disease even if the diagnosis
is not suspected before initiation of thiazide.
2
Fatigue and malaise may be the initial manifestations of
an apathetic form of hyperthyroidism that is found espe-
cially in elderly patients. Hyperthyroidism can produce
mild hypercalcemia, which is found in one fourth of pa-
tients with hyperthyroidism. However, blood calcium lev-
els seldom exceed 11 mg/dL.
3
In addition, renal calculi are
distinctly uncommon in a patient with thyrotoxicosis.
4
Hypercalcemia occurs in about 30% of all patients with
MM. Diffuse bone loss and vertebral fractures occur in
most patients. The serum creatinine value is elevated in
more than one half of patients at diagnosis and is higher
than 2.0 mg/dL in approximately one fourth of patients. A
normocytic, normochromic anemia is seen in nearly two
thirds of patients at the time of diagnosis. The presence of
mild anemia, hypercalcemia, acute renal failure, and verte-
bral fracture in our patient suggests MM.
Hypercalcemia that occurs in patients with FHH is
usually mild. Mutations in the calcium-sensing receptor
on the parathyroid cells and kidneys lead to a defective
calcium regulation such that higher than normal calcium
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