Wright Kurin SAA 2012 Final

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  • 8/2/2019 Wright Kurin SAA 2012 Final

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    A Possible Case of Cancer in the Late Prehispanic Peruvian Andes

    1. Introduction

    This cranium, MCH1.2, was excavated from Pukamachay Cave, at the site of Cachi in Andahuaylas, Peru . Theremains pertain to the Chanka culture and date to the early Late Intermediate Period (A.D. 1000-1250). Becausethe cave was badly looted, no post-cranial elements could be associated with the MCH1.2 cranium, and no otherbones exhibited lytic lesions.

    The Chanka culture, which emerged following the collapse of the Wari Empire ca. AD 1000, was a society thatwitnessed high levels of endemic violence, as well as a higher frequency of pathological lesions indicative ofdisease than earlier imperial era populations. Medico-cultural interventions, such as amputation throughdismemberment and trepanation were likely enacted by the Chanka society to cope with novel challenges in theaftermath of collapse and suggest a nuanced, emic understanding of health and disease (Kurin 2012).

    Katherine Wright and Danielle S. Kurin

    4. Conclusions

    While the absence of postcranial elements makes an absolute diagnosis difficult, the nature of thelesions in MCH1.2 can rule out most of the previously detailed conditions.

    Tuberculosis can be ruled out as a cause of the cranial lesions in MCH1.2. First, cranial lesionsusually present in younger individuals, and MCH1.2 is an adult. Furthermore, the lesions present moreextensive resorbtion of the diploe and the outer tables rather than the inner table. The lesions arelarger than 2mm, and do not cross suture lines.

    Langerhans Cell Histiocytosis can also be disregarded, mainly due to its early age of onset. Even so,

    the lesions seen in MCH1.2 are not punched out, and show some signs of reactive bone formationon the margins.

    Multiple myeloma seems a less likely diagnosis than metastatic carcinoma for MCH1.2. All of thelesions seem too large, too varied in size, and not numerous enough to be caused by multiple

    myeloma. The edges are not as sharp and punched out as they would be with a multiple myelomadiagnosis, and there are signs of osteoblastic boney reaction along the m argins.

    Secondary metastatic carcinoma seems to be the most likely cause of the lesions, but is not a definitediagnosis. The largest lesion has an irregular, sharp, lacy margin with osteoblastic activity and exhibitsthe most destruction in the diploe. The other lesions seem to be varied in size and stage. Althoughfurther research and radiographic analysis are needed to make a certain diagnosis, the characteristicsof the lesions and the age of the individual suggest a most probable diagnosis of secondarymetastatic carcinoma in MCH1.2.

    References:Assis, S.C., 2010. Metastatic carcinoma in a 14th-19th century skeleton from Constancia.International Journal of Osteoarchaeology, 20(5), pp.603-620.Buikstra, J.E. and Ubelaker, D.H., 1994. Standards for data collection from human skeletal remains: Proceedings of a seminar at the Field Museum of Natural History.Arkansas Archeological Survey Research Series, 44.Kurin, D., 2012.The bioarchaeology of collapse: Ethnogenesis and ethnocide in post-imperial Andahuaylas Peru. Unpub. PhD. Vanderbilt University.Marks, M.K. and Hamilton, M.D., 2007.Metastatic carcinoma: Palaeopathology and differential diagnosis.International Journal of Osteoarchaeology,17, pp.217-234.Ortner, D.J., 2003.Identification of pathological conditions in human skeletal remains. San Diego: Academic Press.Rothschild, B.M., Hershkovitz, I. and Dutour, O., 1998.Clues potentially distinguishing lytic lesions of multiple myeloma from those of metastatic carcinoma. American Journal of Physical Anthropology, 105, pp.241-250.Smith, M.O., 2002. A probable case of metastatic carcinoma from the Late Prehistoric Eastern Tennessee River Valley.International Journal of Osteoarchaeology, 12, pp.235-247.

    Acknowledgements: This project was supported by Fulbright-Hays and Vanderbilt University. Special thanks to the ProyectoBioarqueologico Andahuaylas crew including Enmanuel Gomez, Edison Mendoza Martinez, Anna Schneider, Kirsten Green, KirstenDelay, and Jasmine Kelly. Thanks also to Dr. Rebecca Gowland of Durham University and Dr. Don Brothwell of the University of York.

    2. Materials and Methods

    The sex and age of the individual were estimated using standards outlined by Buikstra and Ubelaker (1994).Dental eruption, dental wear, and cranial suture closure indicate the individual was between 35 and 40 at thetime of death. Sex was determined as male based on the rugosity of the mastoid process, nuchal crest,supraorbital margin, and glabella.

    The largest lesion is located superior to and intersecting the right supraorbital margin. The lesion penetrates theinner table, diploe, and outer table of the skull. Destruction is the most extensive in the diploe, and more

    extensive in the outer table than the inner. table Two other lytic foci are evident: a smaller depressed area25.4mmabove the left suprarobital margin with a pinprick hole in the center, and a larger depressed area on theright parietal. Both these lesions present as depressions in the cranium, and the most extensive osteoclasticactivity in the largest lesion is present in the diploe, suggesting the cause of the lesions originated within thediploe. There is new woven bone on the outer margins of the lesion.

    Fig.3:Second lesion on the left frontal bone showing new bonegrowth and a pinprick hole perforating the outer table.

    Wright,2011

    Wright,2011

    Wright,2011

    Department of Archaeology, Durham University; Department of Anthropology, Vanderbilt University

    77th Annual Meeting ofthe

    Societyfor AmericanArchaeology

    April 18-22, 2012

    Memphis, TN

    Fig. 1: Map of Peru showing the location of the Cachi site.

    Fig.4:Active lytic lesion on the right frontal bone of MCH1.2 showing extensive damage to thediploe and reactive bone formation along the margins.

    Fig.5:Pathological cranial lesions present in among Chanka populations in Andahuaylas. From left to right: porotic hyperostosis, periosteal reaction from a healingtrepanation, degraded unhealed trepanation, healing trauma, and the lytic lesion from MCH1.2

    Fig.10:Right lateral view of MCH1.2

    Fig.2:Third lesion on the right parietal demonstratingnew bone growth and a pinprick hole perforating the

    outer table.

    TuberculosisTuberculosis is an infectious disease caused by the mycobacterium tuberculosiscomplex. Once the body detects the bacterias presence, it initiates an aggressiveimmune response that could affect nearby organ tissues. Pathognomic changes oftuberculosis are most commonly seen in the vertebral column, but associated lesionscan also be seen in the skull. Cranial lesions are most commonly seen in subadults

    younger than 10, and are characterized by a round lytic focus of no more than 2 cm in

    diameter, perforation of both inner and outer tables, and commonly crossing suturelines. When seen in adults, cranial lesions usually have more extensive resorption ofthe inner table than the outer and the formation of a sequestrum (Ortner, 2003).

    Langerhans Cell HistiocytosisLangerhans Cell Histiocytosis (LCH) is a disease in which a proliferation ofLangerhans cells (immune cells called histiocytes) leads to increased phagocyticactivity, which can cause lytic lesions if the bone tissues are affected. LCH is most

    frequently seen in the skull, and generally affects subadults between the ages of 0and 15. Lesions in the bone are usually lytic, without reactive bone formation, smalland round, and may coalesce to create a geographic border (Ortner, 2003). Theedges of LCH lesions are usually punched out, meaning sharply defined andcircular, with scalloped edges (Marks and H amilton, 2007; Rothschild et al., 1998).

    Multiple MyelomaMultiple myeloma is a type of cancer in which plasma cells undergo malignanttransformation and growth. The malignant plasma cells secrete a substance thattriggers osteoclastic activity and inhibits osteoblastic activity (Rothschild et al., 1998;Marks and Hamilton, 2007). Therefore, reactive bone growth is not typically seen incases of multiple myeloma. Lesions typically appear as sharply defined, multiple,spherical, small (3-10mm), consistently sized, punchedout holes that penetrate allcranial tables and rarely show remodeled margins. The prevalence of multiple

    myeloma increases with age and is generally seen in older adults.

    Secondary Metastatic CarcinomaThe most common cause of tumors affecting the skeleton is metastasis from other organs(Ortner, 2003). In secondary metastatic carcinoma, expanding blood-borne tumorous cells

    can grow and displace cancellous bone, eventually piercing the cortex and exposing thediploe (Assis, 2010; Smith, 2002). Secondary metastatic carcinoma is most commonlyseen in adults and the elderly. Metastatic tumors to bone are most commonly osteolytic, butmay also be osteoblastic or a mix of both. Lesions tend to be well-defined, and spherical inshape with an ellipsoid component or geographic (irregular) boundary. Lesions vary in

    size, and sometimes have raised margins (Ortner, 2003; Rothschild et al., 1998, p.244).

    3. Differential Diagnosis

    Fig. 7:Multiple punched out lesions

    of multiple myeloma.

    Fig. 9:Osteolytic lesion of secondarymetastatic carcinoma with reactivebone and raising on the margins.

    Fig. 8:LCH lesions showing geographicshape and little reactive bone formation.

    Fig. 6:Lesion of tuberculosis showingpenetration of both tables and formation of

    a sequestrum .

    Marksand Hamilton,2007

    Images below fromOrtner,2003

    Abstract

    The cranium of a 35-40 year old adult male from the Chanka culture (AD 1000-1400) was excavated from the site of Cachi in Andahuaylas, Peru. The cranium presents lesions on the frontal and parietal bones. The osteolytic nature ofthree of the lesions suggested they may be the effect of a treponemal or neoplastic disease. Based on the shape and nature of the lesions, the age and sex of the individual, and the number of lesions, a differential diagnosis is presentedthat includes tuberculosis, Langerhans Cell Histiocytosis, multiple myeloma, and metastatic carcinoma. Ultimately, the lesions seen in MCH1.2 seem most likely to be caused by secondary metastatic carcinoma.