Pulmonary Langerhans Cell Histiocytosis in an African Lion: A Rare Case Report

Author:

Zhang Liang123,Chen Hui123,Ding Yulin123,Wang Wenlong123,Wa Gao45,Zheng Bingwu6,Wang Jinling123ORCID

Affiliation:

1. College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China

2. Key Laboratory of Clinical Diagnosis and Treatment Techniques for Animal Disease, Ministry of Agriculture and Rural Affairs, Hohhot 010018, China

3. Inner Mongolia Autonomous Region Key Laboratory of Veterinary Fundamentals and Disease Prevention and Control of Herbivorous Livestock, Hohhot 010018, China

4. Inner Mongolia Autonomous Region Key Laboratory of Tick-Borne Zoonotic Infectious Disease, Bayan Nur 015000, China

5. Department of Medicine, College of Hetao, Bayan Nur 015000, China

6. Hohhot Zoo, Hohhot 010050, China

Abstract

Background: Feline pulmonary Langerhans cells histiocytosis (PLCH) is a rare disorder that results in progressive respiratory failure secondary to pulmonary parenchymal infiltration with Langerhans cells (LCs). A diagnosis of PLCH is proposed based on the clinical features and pathological findings and confirmed based on the infiltrating histiocytic cells. There are few documented cases of feline PLCH, and this case report of PLCH in an African Lion could present new information and aspects of this feline histiocytic disease. Case presentation: An African lion at Hohhot Zoo showing severe hyporexia and dyspnea with subsequent mental depression and emaciation died of exhaustion after a 35-day course of illness. Empirical treatment did not have a significant effect. An autopsy revealed that the lungs were enlarged and hardened due to infiltrative lesions, with many yellowish-white foci in all the lobes and sections. Furthermore, the kidneys were atrophied and had scattered grayish-white lesions on the surface. At the same time, congestion was widely distributed in various locations, including the liver, subcutaneous loose connective tissues, serosal surface and other tissues and organs. Histologically, proliferative histiocytic cells (PHCs) were scattered in the alveolar cavities, bronchioles and submucosa of bronchioles, with evident cellular and nuclear pleomorphism, and thus the alveolar septa were obliterated. The histopathological changes in other organs included chronic sclerosing glomerulonephritis, proliferated Kupffer cells in the liver, adrenal edema and interstitial connective tissue hyperplasia, as well as atrophy of the small intestines and spleen. Furthermore, immunohistochemical analysis results were strongly positive for CD1a, vimentin, S100 and E-cadherin in the membrane or cytoplasm of PHCs, supporting an LC phenotype. Conclusions: Here, we present a rare pulmonary Langerhans cell histiocytosis case in an African lion.

Funder

Major Science and Technology Projects of Inner Mongolia Autonomous Region

Basic Research Funds for Universities Directly Under the Inner Mongolia Autonomous Region

Discipline Project of College of Veterinary Medicine, Inner Mongolia Agricultural University

National Natural Science Foundation of China

Publisher

MDPI AG

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