After a period in which neurology and psychiatry have become more and more defined, neurologists' interest in psychiatric topics, and vice versa, has increased. This book provides readers with an overview of the most representative neuropsychiatric syndromes such as Ganser and Capgras syndromes. It fills an existing gap in current literature and reintroduces a clinical approach. Additionally, there is a historical perspective throughout time with a focus on the most relevant clinical syndromes, offering distinct value to readers. With this approach, the book serves as a useful and stimulating guide on the diagnosis and management of neurologic psychiatric syndromes. It is for neurologists, neurosurgeons, psychiatrists, and all others interested in neuropsychiatric topics because these syndromes also called 'uncommon' may in fact be more frequent than the literature suggests.

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Publisher

S. Karger

Year

2017

Print ISBN

9783318058581

eBook ISBN

9783318058598

Topic

Medicine

Subtopic

Psychiatry & Mental Health

Bogousslavsky J (ed): Neurologic-Psychiatric Syndromes in Focus. Part I – From Neurology to Psychiatry. Front Neurol Neurosci. Basel, Karger, 2018, vol 41, pp 77–89 (DOI: 10.1159/000475721)

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The Klüver-Bucy Syndrome

Douglas J. Lanska^{a, b}

^aVA Medical Center, Great Lakes VA Healthcare System, Tomah, WI, and ^bDepartment of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA

______________________

Abstract

In 1937, Heinrich Klüver and Paul Bucy described a dramatic behavioral syndrome in monkeys after bilateral temporal lobectomy. The full Klüver-Bucy syndrome (KBS) – hyperorality, placidity, hypermetamorphosis, dietary changes, altered sexual behavior, and visual agnosia – is evident within 3 weeks following operation. Some KBS features (i.e., hyperorality, placidity, hypermetamorphosis) persist indefinitely, whereas others gradually resolve over several years. Klüver and Bucy were initially unaware of an earlier report of KBS by Sanger Brown and Edward Schäfer in 1888. Human cases were recognized in the 1950s, as surgeons employed bilateral temporal lobectomies to treat seizures. Various attempts were made to localize the component features to specific areas of the temporal lobe, with mixed success. Bilateral ventral temporal ablations and bilateral temporal lobectomies produced marked impairment in visual discrimination, whereas lateral resections or unilateral lesions did not. Discrete bilateral lesions of the lateral amygdaloid nucleus produced a permanent “hypersexed state.” By the 1970s, it was clear that the major symptoms of KBS are produced by destroying either the temporal neocortex or the amygdala bilaterally. KBS is now thought to be caused by disturbances of temporal portions of limbic networks that interface with multiple cortical and subcortical circuits to modulate emotional behavior and affect. The clinical features of KBS in man are similar to those in monkeys, but the full syndrome is rarely seen, probably because the anterior temporal lobe dysfunction is usually less severe than that following total temporal lobe ablation in monkeys. Human KBS does not occur in isolation, but is typically part of a complex behavioral syndrome that almost always includes amnesia and aphasia, and that may also include dementia and seizures. The treatment of KBS is difficult and often unsatisfactory.

Introduction and History

In 1937, German-born American psychologist Heinrich Klüver (1897–1979) and American neurosurgeon and neuropathologist Paul Clancy Bucy (1904–1992) described a dramatic behavioral syndrome in Rhesus monkeys that had undergone bilateral temporal lobectomy [1–13]. This was an unanticipated consequence of Klüver’s studies of the reactions of humans and animals to mescaline, a naturally occurring psychedelic alkaloid similar in its effects to LSD.

In an obituary of Klüver, fellow psychologist William A. Hunt (1903–1986) recounted how Klüver became bored after a few days away from his laboratory while on vacation on a New Hampshire farm:

[Klüver] began investigating the effects of mescal on the farmer’s cow. He overestimated the ameliorating effects of body weight on dosage size and the cow died. Klüver confessed his guilt and reimbursed the farmer, but as Klüver said, “He took it unpleasantly.” Klüver also used himself as a subject and consequently suffered an attack of mescal poisoning that left him seriously ill for a while [11, p 160].

As noted in a later biographical memoir, while Klüver was “at the University of Minnesota around 1924, he ingested mescal buttons and compulsively documented the nature of his own experiences during intoxicated states” [13]. Klüver’s later work with mescaline produced behavioral manifestations in monkeys that suggested to him that this drug might act on the temporal lobe:

Our interest in temporal lobe functions was aroused by the discovery of one of us (Klüver) that the injection of mescaline or chemically related substances into monkeys produces peculiar chewing and licking movements as well as convulsions, in other words, symptoms resembling those found in the “uncinate group of fits” described [in 1899] by [English neurologist John] Hughlings Jackson [1835–1911] and [Scottish neurologist James Purves] Stewart [1869–1949]. It was thought desirable, therefore, to remove the temporal lobes, including the uncus [3, pp 989–990].

On this basis, Klüver induced Bucy to perform staged bilateral temporal lobe resections on monkeys to assess whether the effects of mescaline would be ameliorated. On December 7, 1936, Bucy removed most of the left temporal lobe of an aggressive adult female Rhesus monkey named “Aurora” [7, 10, 13]. As Bucy later recounted, the following morning Klüver called him on the telephone and abruptly demanded to know, “What did you do to my monkey?” [10]. Bucy hurried to the office and observed that the once-aggressive monkey had become “tame,” a behavioral change that was even more pronounced after Bucy removed the opposite temporal lobe in a subsequent operation on January 25, 1937 [7, 10, 13].

The initial report by Klüver and Bucy in April 1937, presented at the annual meeting of the American Physiological Society in Memphis, Tennessee, described the effects of sequential staged bilateral temporal lobectomy in an adult Rhesus monkey:

The animal does not exhibit the reactions generally associated with anger and fear. It approaches humans and animals, animate as well as inanimate objects without hesitation and although there are no motor defects, tends to examine them by mouth rather than by the use of hands. There is a general slowing down of movements; the quick, jerky movements characteristic of the normal Rhesus monkey have almost entirely disappeared [1, p 352].

Although the monkey had no impairment in visual acuity or in the ability to visually localize the positions of objects, it seemed unable to recognize objects by sight:

Table 1. Klüver-Bucy syndrome in monkeys

Permanent manifestations

1Hyperorality (marked oral examination of objects with licking, sucking, chewing movements, and placing of non-food objects in the mouth)

2Placidity

3Hypermetamorphosis (constant manual exploration and inappropriate attention to new stimuli)

Temporary manifestations

4Dietary changes (hyperphagia, pica, coprophagia)

5Altered sexual behavior (autosexual, heterosexual, homosexual)

6Sensory agnosias (“psychic blindness”)

The hungry animal, if confronted with a variety of objects, will, for example, indiscriminately pick up [various objects, including uncharacteristically a live snake]. Each object is transferred to the mouth and then discarded if not edible. … These symptoms of what appears to be “psychic blindness” are not present in four other monkeys … in which only one temporal lobe has been removed [1, p 353].

As Klüver and Bucy subsequently elaborated, the full Klüver-Bucy syndrome (KBS) – hyperorality, placidity, hypermetamorphosis, dietary changes, altered sexual behavior, and visual agnosia (Table 1) – is evident within 2–3 weeks following operation [3, 5, 6]. Hyperorality was manifest by a marked tendency to place non-food objects in the mouth, and to examine objects orally (e.g., by licking, sucking, biting, or chewing). Hypermetamorphosis referred to constant manual exploration and inappropriate attention to new stimuli, characterized by an immediate motor response upon the visual presentation of an object, regardless of its history or reward value. The term “hypermetamorphosis” had been coined in 1859 by Breslau psychiatrist Heinrich Wilhelm Neumann (1814–1884), and then adopted and propounded by his assistant, German neuropsychiatrist Carl Wernicke (1848–1905), whose later monograph, Grundriss der Psychiatrie in klinischen Vorlesungen (Outline of Psychiatry in Clinical Lectures, 1906), conveyed the term and concept to Klüver [14]. Dietary changes of KBS included hyperphagia, pica, coprophagia, and ingestion of large quantities of meat (in normally vegetarian monkeys) [3, 5, 6]. Altered sexual behavior was manifest by a marked increase in the frequency and variety (i.e., autosexual, heterosexual, homosexual) of sexual activity, and also in a broadening of stimuli that would precipitate sexual excitation. What Klüver and Bucy initially called “psychic blindness” and later sensory agnosia [1, 3] referred to the apparent inability to recognize and detect the meaning or significance of objects by sight in the absence of any evident impairment in visual acuity or ability. They found that some features of KBS (i.e., hyperorality,...

Cover Page
Front Matter
Minor Hemisphere Major Syndromes
Phantom Sensations, Supernumerary Phantom Limbs and Apotemnophilia: Three Body Representation Disorders
Misoplegia
Pali and Echo Phenomena: Symptoms of Persistence and Perseveration
Pathological Yawning, Laughing and Crying
Catastrophe Reaction and Emotionalism
Addictive (Non-Drug) and Obsessive-Compulsive Symptoms after Focal Brain Lesions
Hypersexuality in Neurological Disorders: From Disinhibition to Impulsivity
The Klüver-Bucy Syndrome
Diogenes Syndrome
Brueghel Syndrome or Meige Syndrome? Two Sides of a Same Disease
REM Sleep Behavior Disorder: A Unique Window into Dreaming, the Violent Brain and Early Mechanisms of Neurodegeneration
Charles Bonnet Syndrome and Other Hallucinatory Phenomena
Author Index
Subject Index
Back Cover Page

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Neurologic-Psychiatric Syndromes in Focus - Part I

From Neurology to Psychiatry