Thunderclap headache without hypertension in a patient with pheochromocytoma
© Springer-Verlag 2010
Received: 12 April 2010
Accepted: 6 June 2010
Published: 13 July 2010
Pheochromocytoma is a well known, catecholamine-producing tumor characterized by hypertension, headache, hyperglycemia, hypermetabolism, and hyperhydrosis. Approximately 65% of cases of pheochromocytoma were shown to be associated with hypertension. A case of pheochromocytoma that presented with thunderclap headache (TCH) and palpitations is reported. The patient never showed hypertension during the course of the disease. Paroxysmal headache and palpitations led to the identification of the underlying condition, and the final diagnosis was confirmed by histopathological examination of a surgical specimen. Pheochromocytoma should be identified as a less common although important cause of TCH. In addition, due to its lack of utility in identifying this disorder, negative cranial imaging may impede further investigation of extracranial lesions that may be the cause of a patient’s headache. According to the International Classification of Headache Disorders (ICHD)-II, headache attributed to pheochromocytoma usually develops concomitantly with an abrupt increase in blood pressure. In our case, however, hypertension was never observed, even when the patient was symptomatic. This is the first report of a case of pheochromocytoma with TCH without hypertension.
Thunderclap headaches (TCHs) is characterized by a sudden onset of severe head pain that peaks within 1 min of onset. Although benign primary TCHs are described in the International Classification of Headache Disorders-II, TCHs are considered to be symptomatic of subarachnoid hemorrhages, and their importance in diagnosis of acute illness by exclusion is specially mentioned. In a case with a chief complaint of sudden headaches, we succeeded in detecting the presence of a pheochromocytoma because of the accompanying palpitations. There is a danger of laxness in the differential diagnosis of TCH cases once the possibility of subarachnoid hemorrhage is excluded. We present a case that may affect the long-term prognosis of TCH patients in which the decisive factor in the differential diagnosis of TCH was detected by abdominal imaging rather than head imaging.
A patient was a 33-year-old Japanese woman.
Sudden intense headaches and palpitations.
Past medical history
The patient had experienced migraines without aura, since her early 20s. She had right ovarian cysts resected at 26 years of age and a myomectomy at 32 years of age.
No family history of headaches, thyroid tumor, or hyperparathyroidism was present.
Current medical history
On the 10th of 10 years, while resting after lunch, the patient experienced sudden intense palpitations immediately followed by a severe pulsating headache. Although there was no nausea or vomiting, the patient described it as the “worst headache of my entire life.” After continuing for about 1 h, the headache gradually disappeared with rest. Because a similar attack occurred on the following day, the patient was seen at the neurosurgery department at her local hospital 2 days after initial occurrence. A cranial CT scan was performed on the same day. Owing to the relatively short duration of her headache, negative neurological examination, and negative brain CT scan, the patient was judged to have no abnormalities or need a lumbar puncture. The neurosurgeon prescribed loxoprofen, etizolam, but there was not much effect.
After 10 days of examination, the patient underwent an outpatient migraine examination because of similar, frequent and intense headaches.
The patient had a normal blood pressure and heart rate on physical examination. There were no special neurological findings.
The patient’s blood pressure was within the normal range for the duration of this study, including during both headache occurrence and non-occurrence. There were seven headache during hospitalization of 18 days. The average blood pressure for this time period was 112.6/66.0 mmHg; no evidence of hypertension was observed. The average heart rate during headache occurrence was 88.0 bpm; however, the patient reported experiencing palpitations three times. We administered prazosin hydrochloride and nifedipine to restore her circulating blood volume. A laparoscopic adrenalectomy was performed 2 months later, and a macroscopically well defined, solid tumor measuring 3 × 3 × 2.7 cm was found in the left adrenal gland.
The tumor consisted of solid and fascicular proliferation of polygonal and rhombic cells. The tumor cells had hyperchromatic round nuclei with a rough chromatin pattern and basophilic cytoplasm. On immunohistochemical analyses, the tumor cells were positive for CD56, chromogranin A, and synaptophysin. From these results, the tumor was diagnosed as a pheochromocytoma.
Thunderclap headaches occur suddenly, with pain intensity peaking in under 1 min and continuing from 1 h to 10 days. The most dangerous condition associated with headaches meeting these criteria is subarachnoid hemorrhage; however, numerous other diseases involving the vasculature of the central nervous system, such as ischemic stroke , cerebral venous thrombosis, cervical artery dissection, acute hypertensive crisis, retroclival hematoma, pituitary apoplexy and non-vascular structure of the central nervous system, such as spontaneous intracranial hypotension, third ventricle colloid cyst, and intracranial infection  are found on the list of diseases that should be excluded in the differential diagnosis. Therefore, TCH is a particularly important symptom in differential diagnosis by cranial imaging. However, it is extremely important to bear in mind that many other diseases associated with TCHs, such as pheochromocytoma [3–6] and, myocardial infarction cannot be detected with cranial imaging and may have serious outcomes.
Previously reported cases of TCH with pheochromocytoma
Sanyal and Fletcher 
Sudden, short, excruciating
Pulsating sensation in abdomen and chest
Heo et al. 
Explosive, pulsatile, worst of her life
Im and Kim 
Sudden, pulsating, worst of his life
Sweating, conjunctival injection, restlessness
Sudden, pulsatile, worst of her life
This case study suggests that pheochromocytoma should be included in the differential diagnosis of TCHs with accompanied by palpitations, even when the blood pressure is normal. We would also like to propose that headache occurring concurrently with sudden blood pressure elevation may be inadequate as diagnostic criteria for headaches caused by pheochromocytoma.
Conflict of interest
- Edwardsson BA, Persson S (2009) Cerebral infarct presenting with thunderclap headache. J Headache Pain 10:207–209, 10.1007/s10194-009-0116-4View ArticleGoogle Scholar
- Schwedt TJ, Matharu MS, Dodick DW (2006) Thunderclap headache. Lancet Neurol 5:621–631, 10.1016/S1474-4422(06)70497-5PubMedView ArticleGoogle Scholar
- Im SH, Kim NH (2008) Thunderclap headache after micturition in bladder pheochromocytoma. Headache 48:965–967, 10.1111/j.1526-4610.2008.01031.xPubMedView ArticleGoogle Scholar
- Heo YE, Kwon HM, Nam HW (2008) Thunderclap headache as an initial manifestation of phaeochromocytoma. Cephalalgia 29:388–390, 10.1111/j.1468-2982.2008.01738.xPubMedView ArticleGoogle Scholar
- Udayakumar N, Sivaprakash S, Chandrasekaran M (2007) Headache as the only sign of pheochromocytoma: an analysis. Indian J Med Sci 61:611–613, 1:STN:280:DC%2BD2snovFOqtQ%3D%3D, 10.4103/0019-5359.34966PubMedView ArticleGoogle Scholar
- Sanyal K, Fletcher S (2009) Headache as a sign of phaeochromocytoma. Emerg Med J 26:71, 1:STN:280:DC%2BD1M%2Fgsl2lsQ%3D%3D, 10.1136/emj.2008.059832PubMedView ArticleGoogle Scholar
- Headache Classification Subcommittee of the International Headache Society (2004) The International Classification of Headache Disorders; Edition. Cephalalgia 24(Suppl 1):1–160Google Scholar
- Bravo EL, Tarazi RC, Gifford RW, Stewart BH (1979) Circulating and urinary catecholamine in pheochromocytoma: diagnostic and pathophysiologic implications. N Eng J Med 301:682–686, 1:CAS:528:DyaE1MXlvFWjsrw%3D, 10.1056/NEJM197909273011302View ArticleGoogle Scholar
- Agarwal A, Gupta S, Mishra AK, Singh N, Mishra SK (2005) Normotensive pheochromocytoma: institutional experience. World J Surg 29:1185–1188, 10.1007/s00268-005-7839-4, 16091986PubMedView ArticleGoogle Scholar
- Kitamura K, Kangawa K, Kuwamoto M, Ichiki Y, Nakamura S, Matsuo H (1993) Adrenomedulin: a novel hypotensive peptide isolated from human pheochromocytoma. Biochem Biophys Res Commun 192:553–560, 1:CAS:528:DyaK3sXksVWktb0%3D, 10.1006/bbrc.1993.1451PubMedView ArticleGoogle Scholar